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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167269Generated: November 2, 2026

Benzyl chloroformate → HCID 57105936, compound

https://huagongshe.com/reaction/1167269

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 numberUS06617350B2
Source datasetuspto-grants-2003_09
ORD IDord-3de8066a0f674a1b871b6f4a2aac0070
Source noteuspto-grants-2003_09