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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1524347Generated: November 4, 2026

Benzyl chloroformate → benzyl[(2S)-1-{[tert-butyl(diphenyl)silyl]oxy}-6-hydroxyhexan-2-yl](3-methylbutyl)carbamate

https://huagongshe.com/reaction/1524347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
Reactant(5S)-6-{[tert-butyl(diphenyl)silyl]oxy}-5-[(3-methylbutyl)amino]hexan-1-olHCID 86708047—
SolventChloroformHCID 6212—
Productbenzyl[(2S)-1-{[tert-butyl(diphenyl)silyl]oxy}-6-hydroxyhexan-2-yl](3-methylbutyl)carbamateHCID 8670805067.1%

Reaction Steps

To a stirred solution of the material from Step 5 (8 g, 18.11 mmol) in a 2:1 mixture of chloroform and saturated aqueous NaHCO3 (271 mL) was added benzyl chloroformate (2.59 mL, 118.11 mmol). The reaction mixture was stirred at room temperature for 1 hour, partitioned and extracted with chloroform. The combined organics were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography on silica gel using EtOAc-hexanes (10 to 70%) to yield 7 g of the title compound. LCMS (M+1)=576

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079834B2
Source datasetuspto-grants-2015_07
ORD IDord-2a5b393dc4c34cb6887016cd2e555922
Source noteuspto-grants-2015_07