| Identification | More | [Name]
L-Serine benzyl ester hydrochloride | [CAS]
60022-62-0 | [Synonyms]
H-SER-OBZL HCL
L-SERINE BENZYL ESTER HYDROCHLORIDE
SERINE-OBZL HCL
L-SerinebenzylesterHCl | [Molecular Formula]
C10H14ClNO3 | [MDL Number]
MFCD00038955 | [Molecular Weight]
231.68 | [MOL File]
60022-62-0.mol |
| Chemical Properties | Back Directory | [Melting point ]
175°C | [refractive index ]
-12 ° (C=1, H2O) | [storage temp. ]
−20°C
| [form ]
powder to crystal | [color ]
White to Almost white | [Water Solubility ]
Soluble in water. | [InChI]
InChI=1/C10H13NO3.ClH/c11-9(6-12)10(13)14-7-8-4-2-1-3-5-8;/h1-5,9,12H,6-7,11H2;1H/t9-;/s3 | [InChIKey]
MGZWCDQAKCHOBX-FVGYRXGTSA-N | [SMILES]
C(OCC1=CC=CC=C1)(=O)[C@H](CO)N.[H]Cl |&1:10,r| | [CAS DataBase Reference]
60022-62-0(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Description]
L-Serine benzyl ester hydrochloride, also known as L-Serine-Bz-HCl, is a derivative of the amino acid L-Serine. It is a water-soluble, white crystalline powder and is commonly used as a reagent in biochemical and physiological studies. It is a useful raw material that could synthesize mang organic compounds, such as a cyclic sulfamidate which could reacted cleanly with the sodium thiolate
salt of a variety of unprotected 1-thio sugars in aqueous buffer to afford the corresponding S-linked amino acid glycoconjugates in good
yields after hydrolysis of the N-sulfates[1].
| [Chemical Properties]
Colorless solid | [Uses]
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff. | [Preparation]
Boc-L-Ser-OBz (2.953 g, 10 mmol) was dissolved in MeOH (21 mL) and was palced in ice bath. Then concentrated hydrochloric acid (4.25 mL) was added dropwise. The ice bath was removed and the reaction mixture was stirred for 3 hours. After that the isopropanol (10 mL) was added and the volatile components were removed under reduced pressure at 55 ℃. The oily residue was coevaporated with isopropanol three times (3x10 mL). L-Serine benzyl ester hydrochloride ( yield=69%) was crystallized from H2O/iPr-OH/acetone mixture.
 | [Synthesis]
a) To a 250 mL three-necked flask was added a mixed solution of benzyl alcohol (70 mL) and carbon tetrachloride (70 mL) of L-serine (15.00 g, 0.14 mol) and p-toluenesulfonic acid (29.30 g, 0.15 mol). The reaction mixture was heated to reflux overnight under a Dean-Stark apparatus (a total of 7 mL of water was collected). Upon completion of the reaction, carbon tetrachloride was removed by distillation under reduced pressure. Dichloromethane (50 mL) was added to the residue and the resulting solution was washed sequentially with saturated aqueous sodium bicarbonate (3 x 50 mL) and 1 M hydrochloric acid (3 x 50 mL). The aqueous phases were combined, concentrated under reduced pressure and dried to give L-serine benzyl ester hydrochloride (17.52 g, 54% yield) as colorless crystals with melting point 169-171 °C. LC-MS m/z: 196.15 [M+H]+.
(b) Boc-phenylalanine (2.92 g, 11.00 mmol) was dissolved in N,N-dimethylformamide (50 mL) in a dry 100 mL three-necked flask. N,N-diisopropylethylamine (1.88 mL, 11.00 mmol), 1-ethyl-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.95 mL, 11.00 mmol), and 1-hydroxybenzotriazole (1.49 g, 11.00 mmol) were added sequentially. After stirring at room temperature for 5 minutes, L-serine benzyl ester hydrochloride (2.31 g, 10.00 mmol) was added and the reaction was continued with stirring overnight. After completion of the reaction, the reaction mixture was diluted with ether (150 mL) and washed sequentially with 1 M hydrochloric acid (2 x 100 mL), saturated saline (100 mL), saturated aqueous sodium bicarbonate solution (2 x 100 mL) and saturated saline (100 mL). The organic phase was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The target product (2.08 g, 78% yield) was purified by fast column chromatography using ethyl acetate/hexane (1:1, v/v) as eluent to afford the target product (2.08 g, 78% yield) as a colorless oil. | [References]
[1] Cohen S, et al. Synthesis of S-linked glycosyl amino acids in aqueous solution with unprotected carbohydrates. Organic Letters, 2001; 3: 405–407. |
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