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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046044Generated: October 30, 2026

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

https://huagongshe.com/reaction/1046044

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 numberUS08569292B2
Source datasetuspto-grants-2013_10
ORD IDord-a38230da069a4b229414bf86e5fe0d35
Source noteuspto-grants-2013_10