HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372067Generated: October 30, 2026
Chloroform → 4-Phenylbutanoylmethyltriphenylphosphonium chloride
https://huagongshe.com/reaction/372067
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Chloro-5-phenylpentan-2-one | HCID 12517697 | — |
| Product | 4-Phenylbutanoylmethyltriphenylphosphonium chloride | HCID 86735705 | — |
Reaction Steps
A solution of 1-chloro-2-oxo-5-phenylpentane (6.55 g.) in dry chloroform (30 ml.) was added to a solution of triphenylphosphine (8.7 g.) in dry chloroform (30 ml.) and heated at reflux in an atmosphere of dry nitrogen for 4 hours. The solution was then evaporated under reduced pressure and the residual oil was triturated with a mixture of light petroleum ether (b.p. 40°-60° C.) and diethyl ether, to give a white solid. Recrystallisation of this material from a mixture of dichloromethane and diethyl ether gave 4-phenylbutanoylmethyltriphenylphosphonium chloride (11.2 g.) in the form of a white crystalline solid. m.p. 192-195° C. (Elemental analysis: C, 76.0; H, 6.2%; C29H28ClOP requires: C, 75.9; H, 6.2%; νmax 1110 cm-1, 1445 cm-1, 1490 cm-1, 1695 cm-1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04088695 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-fe8e53098cce4cb08714b39b96f74b62 |
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| Source note | uspto-grants-1978_05 |
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