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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470404Generated: October 29, 2026

Ammonium Chloride → 1-Chloro-3-(4-fluorophenyl)-5-methylhex-5-en-3-ol

https://huagongshe.com/reaction/470404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Chloro-4'-fluoropropiophenoneHCID 67672—
Reactant3-Iodo-2-methylprop-1-eneHCID 10877752—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
Product1-Chloro-3-(4-fluorophenyl)-5-methylhex-5-en-3-olHCID 5963567476%

Reaction Steps

A solution of 3-chloro-1-(4-fluorophenyl)-propan-1-one (18.6 g, 0.1 mol) in THF (50 mL) was added to a well-stirred suspension of zinc power (13 g, 0.2 mol) in a mixture of aqueous saturated NH4Cl solution (260 mL) and THF (65 mL). A solution of 3-iodo-2-methylprop-1-ene (36.4 g, 0.2 mol) in THF (50 mL) was added dropwise. The reaction mixture was mildly exothermic, and began to reflux spontaneously. After the refluxing had ceased, the mixture was stirred for 1 h. TLC showed the 3-chloro-1-(4-fluorophenyl)propan-1-one not reacted completely. A solution of 3-iodo-2-methylprop-1-ene (18.2 g, 0.1 mol) in THF (30 mL) was added, and the mixture was stirred at rt overnight. The mixture was extracted with EtOAc (2×500 mL). The combined organic layer was dried and concentrated. The residue was purified by column chromatography on silica gel eluted with petroleum ether/EtOAc 50:1→30:1→5:1, to give 1-chloro-3-(4-fluorophenyl)-5-methylhex-5-en-3-ol (17 g, yield 76%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629138B2
Source datasetuspto-grants-2014_01
ORD IDord-4f38b12f117245faa36a886666dabb76
Source noteuspto-grants-2014_01