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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457458Generated: November 1, 2026

Allyl bromide → HCID 66853728, compound

https://huagongshe.com/reaction/1457458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
Reactant(2S,4R)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acidHCID 88804—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66853728HCID 6685372846.1%

Reaction Steps

N-tert-Butoxycarbonyl(4R)-hydroxyproline (9.25 g, 40 mmol) was added to a solution of 60% sodium hydride (3.36 g, 84 mmol) in 100 ml of anhydrous tetrahydrofuran and stirred for 2 hours at room temperature. Allyl bromide (6.9 ml, 80 mmol) was added to the mixture and refluxed for 6 hours. The mixture was quenched with the addition of ice chips, then additional water was added and the mixture was washed with hexane. The aqueous layer was acidified with 10% sodium hydrogen sulfate and extracted with ethyl acetate (2×150 ml). The combined extracts were dried over anhydrous sodium sulfate, filtered and evaporated to give 5 g of the title product with no further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05847135
Source datasetuspto-grants-1998_12
ORD IDord-216b2ccdffa24e15a80018d6795f77b1
Source noteuspto-grants-1998_12