| Identification | Back Directory | [Name]
(R)-3-HYDROXYMETHYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER | [CAS]
138108-72-2 | [Synonyms]
N-Boc-D-^b-prolinol
N-Boc-D-beta-prolinol
N-Boc-D-^b-prolinol, 97+%
(R)-1-Boc-3-(hydroxyMethy...
(R)-1-Boc-3-pyrrolidineMethanol
(R)-N-BOC-PYRROLIDINE-3-METHANOL
[R]-1-BOC-3-Pyrrolidinemethanol 97%
(R)-1-Boc-3-hydroxymethylpyrrolidine
1-Boc-3(R)-(HydroxyMethyl)Pyrrolidine
(3R)-1-Boc-3-(hydroxymethyl)pyrrolidine
(R)-3-hydroxyMethyl-pyrrolidine-1-carboxylic
(R)-1-tert-Butoxycarbonylpyrrolidine-3-methanol
(3R)-N-tert-butyloxycarbonyl-3-hydroxymethylpyrrolidine
tert-butyl(R)-3-(hydroxymethyl)pyrrolidine-1-carboxylate
tert-butyl (3R)-3-(hydroxyMethyl)pyrrolidine-1-carboxylate
3(R)-HYDROXYMETHYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
(R)-3-HYDROXYMETHYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
(3R)-3-(Hydroxymethyl)pyrrolidine-1-carboxylic acid tert-butyl ester
1-Pyrrolidinecarboxylic acid, 3-(hydroxymethyl)-, 1,1-dimethylethyl ester, (3R)- | [EINECS(EC#)]
1592732-453-0 | [Molecular Formula]
C10H19NO3 | [MDL Number]
MFCD03094725 | [MOL File]
138108-72-2.mol | [Molecular Weight]
201.26 |
| Chemical Properties | Back Directory | [Boiling point ]
289.5±13.0 °C(Predicted) | [density ]
1.089 | [storage temp. ]
Sealed in dry,2-8°C | [solubility ]
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) | [form ]
Oil | [pka]
14.93±0.10(Predicted) | [color ]
Clear Colourless to Pale Yellow | [Optical Rotation]
Consistent with structure | [Water Solubility ]
Slightly soluble in water | [InChI]
InChI=1S/C10H19NO3/c1-10(2,3)14-9(13)11-5-4-8(6-11)7-12/h8,12H,4-7H2,1-3H3/t8-/m1/s1 | [InChIKey]
HKIGXXRMJFUUKV-MRVPVSSYSA-N | [SMILES]
N1(C(OC(C)(C)C)=O)CC[C@@H](CO)C1 | [CAS DataBase Reference]
138108-72-2 |
| Hazard Information | Back Directory | [Uses]
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs. | [Synthesis]
Borane-THF complex (1.0 M, 17 mL, 16.9 mmol) was added slowly and dropwise to a stirred solution of (R)-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acid (1.21 g, 5.6 mmol) in tetrahydrofuran (THF, 30 mL) at 0 °C. The reaction mixture was gradually warmed to room temperature over 30 minutes, followed by heating at 45 °C for 1 hour and then at 55 °C for 90 minutes. Upon completion of the reaction, the mixture was cooled to 0 °C and quenched by careful addition of 3N hydrochloric acid (30 mL). After stirring for 20 min at room temperature, the reaction mixture was extracted with ether (Et2O, 50 mL). The organic layer was washed sequentially with saturated aqueous sodium bicarbonate (NaHCO3, 20 mL) and brine (20 mL), dried over anhydrous sodium sulfate (Na2SO4), filtered, and concentrated under reduced pressure to afford (R)-tert-butyl-3-(hydroxymethyl)pyrrolidine-1-carboxylate (1.1 g, 91% yield) as a colorless oil. | [References]
[1] Patent: WO2011/150198, 2011, A1. Location in patent: Page/Page column 151
[2] Patent: WO2010/45212, 2010, A2. Location in patent: Page/Page column 299
[3] Patent: US2013/184313, 2013, A1. Location in patent: Paragraph 1541 |
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