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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470398Generated: October 30, 2026

3-Chloropropiophenone → 1-Chloro-3-phenylhex-5-en-3-ol

https://huagongshe.com/reaction/470398

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChloropropiophenoneHCID 70295—
ReactantHCID 178455850HCID 178455850—
SolventTetrahydrofuranHCID 8028—
Product1-Chloro-3-phenylhex-5-en-3-olHCID 1593347586%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 3-chloro-1-phenylpropan-1-one (170 g, 1.01 mol) in anhydrous THF (1200 mL) was added allylmagnesium bromide (1.2 L, 1 mol/L) at −78° C. under nitrogen. The formed mixture was stirred for 30 min at −78° C. The reaction was quenched with aqueous NaHCO3 solution. The organic phase was separated, dried over Na2SO4 and concentrated to give the crude product, which was purified by column chromatography (petroleum ether/EtOAc=100:1) to afford 1-chloro-3-phenylhex-5-en-3-ol (180 g, 86%). 1H NMR (CDCl3): 2.27 (m, 2H), 2.51 (m, 1H), 2.74 (m, 1H), 3.22 (m, 1H), 3.58 (m, 1H), 5.16 (m, 2H), 5.53 (m, 1H), 7.23 (m, 1H), 7.39 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629138B2
Source datasetuspto-grants-2014_01
ORD IDord-3561cd09a6a04c60b5cf2384c518ae10
Source noteuspto-grants-2014_01