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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206610Generated: November 2, 2026

Chloroacetone → 1-(Triphenylphosphoranylidene)acetone

https://huagongshe.com/reaction/2206610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetoneHCID 6571—
ReactantTriphenylphosphineHCID 11776—
SolventChloroformHCID 6212—
Product1-(Triphenylphosphoranylidene)acetoneHCID 1503823.3%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371331B2
Source datasetuspto-grants-2016_06
ORD IDord-2af0e805b7fd4440875f3a6817f05fd3
Source noteuspto-grants-2016_06