HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206610Generated: November 2, 2026
Chloroacetone → 1-(Triphenylphosphoranylidene)acetone
https://huagongshe.com/reaction/2206610
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-(Triphenylphosphoranylidene)acetone | HCID 15038 | 23.3% |
Reaction Steps
A solution of 1-chloropropan-2-one (50 g, 540.4 mmol) in chloroform (150 mL) was added dropwise to a solution of triphenylphosphine (141.72 g, 540.4 mmol) in chloroform (150 mL) under nitrogen. The mixture was stirred at 70° C. for 12 hr, and the resulting phosphonium salt was filtered. The precipitate was washed with ethyl acetate and dried under vacuum. The dried phosphonium salt was suspended in a mixture of water (250 mL) and methanol (250 mL), and the mixture was stirred for 1 hr. Aqueous sodium hydroxide (2.00 M) was added to the mixture until a pH between 7 and 8 was reached. The mixture was then stirred vigorously for 1 hr. The phosphorane precipitate was filtered and washed with water. After drying in vacuum, the phosphorane was recrystallized from ethyl acetate and dried under vacuum to afford 1-(triphenylphosphoranylidene)propan-2-one (40.00 g, 23.3%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09371331B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-2af0e805b7fd4440875f3a6817f05fd3 |
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| Source note | uspto-grants-2016_06 |
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