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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895009Generated: October 30, 2026

Benzyl Bromide → HCID 66687435, compound

https://huagongshe.com/reaction/1895009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 66687908HCID 66687908—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66687435HCID 6668743523%

Reaction Steps

Benzyl bromide (0.19 mL, 1.60 mmol) was added to a solution of 3-(3,4-dichloro-benzoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (138 mg, 0.40 mmol) in THF (5 mL), and then lithium bis(trimethylsilyl)amide (1.0 M, in THF, 1.2 mL, 1.20 mmol) was slowly added at room temperature. The reaction mixture was stirred at room temperature for 1.5 hours, then was quenched by addition of saturated aqueous NH4Cl, diluted with water, and extracted with EtOAc. The combined organic extracts were dried over MgSO4, filtered and evaporated under reduced pressure. The residue was purified by flash chromatography (10% to 20% of EtOAc in hexane) to give 40 mg (23% yield) of 3-benzyl-3-(3,4-dichloro-benzoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513425B2
Source datasetuspto-grants-2013_08
ORD IDord-8a6650e36f0d4de4a39bd14101305645
Source noteuspto-grants-2013_08