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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921276Generated: October 30, 2026

Sodium Carbonate → (S)-chloromethyl 2-((tert-butoxycarbonyl)amino)propanoate

https://huagongshe.com/reaction/921276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTert-butoxycarbonylalanineHCID 85082—
ReactantChloromethyl chlorosulfateHCID 2733556—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(S)-chloromethyl 2-((tert-butoxycarbonyl)amino)propanoateHCID 11481803—

Reaction Steps

To a vigorously stirred mixture of (S)-2-((tert-butoxycarbonyl)amino) propanoic acid (1 g, 5.29 mmol), tetrabutylammonium hydrogen sulfate (0.359 g, 1.057 mmol), and Na2CO3 (2.80 g, 26.4 mmol) in DCM 20 (mL) and water (20 mL), cooled in an ice/water bath, was slowly added chloromethyl chlorosulfate (1.09 mL, 10.57 mmol) over a 4 min period. After stirring in an 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. The crude material (1.64 g) was used as is without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273014B2
Source datasetuspto-grants-2016_03
ORD IDord-e508b37085ae4b459d56473779b59086
Source noteuspto-grants-2016_03