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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078504Generated: November 1, 2026

N-bromobutanimide → (3S)-1-bromo-4-(4-fluorophenoxy)-3-hydroxy-1-butyne

https://huagongshe.com/reaction/2078504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3-Butyn-2-ol, 1-(4-fluorophenoxy)-, (2S)-HCID 86588775—
CatalystSilver NitrateHCID 24470—
SolventAcetoneHCID 180—
Product(3S)-1-bromo-4-(4-fluorophenoxy)-3-hydroxy-1-butyneHCID 67096607—

Reaction Steps

A mixture of (3S)-4-(4-fluorophenoxy)-3-hydroxy-1-butyne (2.5 g, 14 mmol), N-bromosuccinimide (NBS) (2.74 g, 15.4 mmol) and AgNO3 (0.12 g, 0.7 mmol) in acetone (70 mL) was stirred at ambient temperature. The pale solution became cloudy over 30 minutes. The mixture was concentrated under vacuum and the resulting residue was filtered through a plug of silica gel (1×5 cm) eluted with 1:4 ethyl acetate:hexane to obtain (3S)-1-bromo-4-(4-fluorophenoxy)-3-hydroxy-1-butyne, a compound of formula (CC), as a pale yellow oil containing some ethyl acetate, 4.75 g (quant.); 1H NMR (CDCl3) δ 3.95-4.15 (m, 2H), 4.75 (m, 1H), 6.86 (m, 2H), 6.97 (m, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928255B2
Source datasetuspto-grants-2011_04
ORD IDord-4adbec656b1a4be2a2fd435be757d52f
Source noteuspto-grants-2011_04