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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675410Generated: October 31, 2026

tert-Butyldimethylsilyl chloride → (1r)-1-{[2(s)-(Hex-5-enyl-methyl-carbamoyl)-4(r)-tert-butyldimethylsilyloxy-pyrrolidine-n-carbonyl]-amino}-2(r)-vinyl-cyclopropanecarboxylic acid ethyl ester

https://huagongshe.com/reaction/1675410

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(1R)-1-{[2(S)-(hex-5-enyl-methyl-carbamoyl)-4(R)-hydroxy-pyrrolidine-N-carbonyl]amino}-2(R)-vinyl-cyclopropanecarboxylic acid ethyl esterHCID 66650543—
SolventDichloromethaneHCID 6344—
Product(1r)-1-{[2(s)-(Hex-5-enyl-methyl-carbamoyl)-4(r)-tert-butyldimethylsilyloxy-pyrrolidine-n-carbonyl]-amino}-2(r)-vinyl-cyclopropanecarboxylic acid ethyl esterHCID 6665052970%

Reaction Steps

Under nitrogen atmosphere, the tert-butyldimethylsilyl chloride was added to a solution of compound 50 (750 mg, 1 eq.) and TEA (537 μL, 1 eq.) in DCM (6 mL). The reaction mixture was stirred overnight at room temperature and quenched with water. The organic layer was washed with brine, dried on sodium sulfate, and concentrated under reduced pressure. The residue was purified by chromatography on silica gel to yield compound 51 in 70% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003659B2
Source datasetuspto-grants-2011_08
ORD IDord-54ca5aaa06104851ae3ea6044ccef7f4
Source noteuspto-grants-2011_08