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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727539Generated: October 29, 2026

Allyl bromide → HCID 19705450, compound

https://huagongshe.com/reaction/727539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 19705499HCID 19705499—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19705450HCID 1970545090%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 3-(2-methylpropyl)-1-trimethylsilyl-2-pyrrolidinone (10.2 g, 47.8 mmol) and THF (153 mL) is cooled to -78° C., and LDA (2.0 M, 26.3 mL, 52.6 mmol) is added. The solution is stirred at -78° C. for 30 minutes and then allyl bromide (5.0 mL, 57 mmol) is added. The solution is allowed to warm to 5° C. over 2.5 hours, and is then stirred at 5° C. for 1 hour. After quenching with saturated aqueous ammonium chloride (25 mL), aqueous workup (EtOAc, MgSO4) and purification by column chromatography (1:9:10 v/v CH2Cl2 :EtOAc:hexane) provides 7.76 g (90%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712300
Source datasetuspto-grants-1998_01
ORD IDord-5aaa048104574debaf0d8af9dff79f49
Source noteuspto-grants-1998_01