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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516443Generated: October 29, 2026

Dichloromethane → chloromethyl (2S)-2-(((tert-butoxy)carbonyl)amino)-3-methylbutanoate

https://huagongshe.com/reaction/516443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBoc-L-ValineHCID 83693—
ReactantSodium BicarbonateHCID 516892—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
Productchloromethyl (2S)-2-(((tert-butoxy)carbonyl)amino)-3-methylbutanoateHCID 54112037—

Reaction Steps

To a mixture of (S)-2-(t-butoxycarbonylamino)-3-methylbutanoic acid (28.6 g, 130 mmol) and NaHCO3 (44 g, 520 mmol) and Bu4NHSO4 (4.4 g, 13 mmol) in DCM (200 mL) and water (200 mL) was added chloromethyl sulfochloridate (26 g, 158 mmol) at 0° C. The mixture was stirred at room temperature for 24 hours, and then was extracted with DCM (3×150 mL). The combined organic layers were washed with water (2×300 mL), and the DCM layer was purified by flash column (petroleum ether:EA=15:1) to yield the title compound as a yellow solid (35 g). LC-MS: 266 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108934B2
Source datasetuspto-grants-2015_08
ORD IDord-63773046c64843d28ce9230623933470
Source noteuspto-grants-2015_08