HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045982Generated: October 30, 2026
Ammonium Chloride → 1-Chloro-3-(4-fluorophenyl)-5-methylhex-5-en-3-ol
https://huagongshe.com/reaction/2045982
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Chloro-4'-fluoropropiophenone | HCID 67672 | — |
| Reactant | 3-Iodo-2-methylprop-1-ene | HCID 10877752 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Chloro-3-(4-fluorophenyl)-5-methylhex-5-en-3-ol | HCID 59635674 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592410B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-c6e7b56f44df48998d72f2fa66af01a2 |
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| Source note | uspto-grants-2013_11 |
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