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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074955Generated: October 31, 2026

Benzyl chloroformate → HCID 57105936, compound

https://huagongshe.com/reaction/2074955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 21356821HCID 21356821—
SolventDichloromethaneHCID 6344—
ProductHCID 57105936HCID 571059364.7%

Reaction Steps

[(1S,2R)-1-Benzyl-3-(4-cyano-2,2-dimethyl-butylamino)-2-hydroxy-propyl]-carbamic acid tert-butyl ester (1.300 g, 3.34 mmol) was dissolved in CH2Cl2 and treated with diisopropylethylamine (1.740 ml, 10.01 mmol) and benzyl chloroformate (0.683 g, 4.00 mmol) at ambient temperature under argon with stirring. After 15 h the reaction mixture was concentrated in vacuo, taken up in EtOAc, washed with sat. aq. NaHCO3, and brine. The organic phase was dried over MgSO4, filtered and solvent removed in vacuo. Purification by column chromatography (10% Et2O in CH2Cl2) gave 0.083 g of a white solid. MS (ES): 524 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919523B2
Source datasetuspto-grants-2011_04
ORD IDord-03c1a08a1f3a46e891a34d3e70e572ed
Source noteuspto-grants-2011_04