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ChemicalBook--->CAS DataBase List--->61644-18-6

61644-18-6

61644-18-6 Structure

61644-18-6 Structure
IdentificationBack Directory
[Name]

Chloromethyl isobutyrate
[CAS]

61644-18-6
[Synonyms]

Chloromethyl isobutyrate
(Isobutyryloxy)methyl chloride
Chloromethyl 2-methylpropanoate
Chloromethyl 2-methylpropionate
Propanoicacid, 2-methyl-, chloromethyl ester
[EINECS(EC#)]

816-730-5
[Molecular Formula]

C5H9ClO2
[MDL Number]

MFCD16038293
[MOL File]

61644-18-6.mol
[Molecular Weight]

136.58
Chemical PropertiesBack Directory
[Boiling point ]

124.6±13.0 °C(Predicted)
[density ]

1.081±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[solubility ]

Chloroform (Sparingly), Methanol (Slightly)
[form ]

Oil
[color ]

Colourless
[InChI]

InChI=1S/C5H9ClO2/c1-4(2)5(7)8-3-6/h4H,3H2,1-2H3
[InChIKey]

ILUWVORABZTBIU-UHFFFAOYSA-N
[SMILES]

C(OCCl)(=O)C(C)C
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS05
[Signal word ]

Danger
[Hazard statements ]

H226-H318
[Precautionary statements ]

P280-P305+P351+P338-P310
[HS Code ]

2915907098
Spectrum DetailBack Directory
[Spectrum Detail]

Chloromethyl isobutyrate(61644-18-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

Chloromethyl chlorosulfate

49715-04-0

Isobutyric acid

79-31-2

Chloromethyl isobutyrate

61644-18-6

Step A: Synthesis of chloromethyl isobutyrate To a solution of isobutyric acid (0.600 mL, 6.47 mmol) in dichloromethane (DCM, 6 mL) was added sodium bicarbonate (2092 mg, 24.91 mmol), tetrabutylammonium hydrogensulfate (220 mg, 0.65 mmol), and water (6 mL) in that order. Chloromethyl chloroformate (0.767 mL, 7.44 mmol) was added slowly at room temperature with rapid stirring. After addition, the reaction mixture was continued to stir at room temperature overnight. Upon completion of the reaction, the reaction mixture was diluted with dichloromethane (10 mL) and subsequently washed with water (2 x 10 mL). The organic phase was dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated to afford the crude chloromethyl isobutyrate (746 mg, 84% yield). The product was used directly in the next step of the reaction without further purification. 1H NMR (500 MHz, CDCl3) δ ppm: 1.17 (m, 6H), 2.62 (m, 1H), 5.72 (s, 2H).

[References]

[1] Patent: WO2015/67923, 2015, A1. Location in patent: Paragraph 00072; 00073; 00074
[2] Patent: US2018/37550, 2018, A1. Location in patent: Paragraph 0081-0083
[3] Patent: WO2014/4884, 2014, A1. Location in patent: Paragraph 00310-00311; 00322
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