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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627590Generated: November 1, 2026

Allyl bromide → N-Boc-O-allyl-L-homoserine

https://huagongshe.com/reaction/627590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
Reactant(2S)-2-(((tert-butoxy)carbonyl)amino)-4-hydroxybutanoic acidHCID 13066457—
SolventDimethylformamideHCID 6228—
ProductN-Boc-O-allyl-L-homoserineHCID 5879866067.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of Boc-L-HomoSer-OH (10.0 g, 45.6 mmol) in DMF was added sodium hydride (2.74 g, 114 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 15 mins, and then allyl bromide (6.90 g, 57.0 mmol) was added. The mixture was warmed to 20° C. and stirred for 2 hrs. The mixture was quenched with saturated NH4Cl solution and then concentrated in vacuum. The residue was diluted with water, and sequentially washed with hexane and ether. The organic layers were discarded, and the aqueous layer was carefully adjusted to pH=3 with 1 N HCl. The acidic aqueous solution was extracted with ethyl acetate. The organic phase was dried over MgSO4 and concentrated in vacuum to give Boc-L-HomoSer(O-allyl)-OH (8.00 g, 67.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309285B2
Source datasetuspto-grants-2016_04
ORD IDord-28edd477a31944629ed68478f3f40267
Source noteuspto-grants-2016_04