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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921275Generated: October 31, 2026

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

https://huagongshe.com/reaction/921275

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantBoc-L-ValineHCID 83693—
ReactantChloromethyl chlorosulfateHCID 2733556—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Productchloromethyl (2S)-2-(((tert-butoxy)carbonyl)amino)-3-methylbutanoateHCID 54112037111.4%

Reaction Steps

To a vigorously stirred mixture of (S)-2-((tert-butoxycarbonyl)amino)-3-methylbutanoic acid (4 g, 18.41 mmol), tetrabutylammonium hydrogen sulfate (1.25 g, 3.68 mmol), and Na2CO3 (9.76 g, 92 mmol) in DCM 80 (mL) and water (80 mL), cooled in an ice/water bath, was slowly added chloromethyl chlorosulfate (3.8 mL, 36.8 mmol) over 4 min. After stirring in the ice/water bath for 30 min, the cold bath was removed and the reaction mixture was allowed to stir at room temperature. After stirring 16 h at room temperature, the reaction mixture was diluted with water and extracted with DCM. The aqueous layer was back extracted with DCM and the combined organic layers were dried over MgSO4, filtered and concentrated to afford Intermediate 38A (5.45 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273014B2
Source datasetuspto-grants-2016_03
ORD IDord-5342d37585c348d587120ba7bde87248
Source noteuspto-grants-2016_03