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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248783Generated: October 25, 2026

Dichloromethane → t-Butyl (triphenylphosphoranylidene)propionate

https://huagongshe.com/reaction/2248783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
Reactanttert-Butyl 2-bromopropanoateHCID 545327—
SolventEthyl AcetateHCID 8857—
Productt-Butyl (triphenylphosphoranylidene)propionateHCID 1091614980.3%

Reaction Steps

The t-butyl (triphenylphosphoranylidene)propionate was prepared as follows: Triphenylphosphine (33 g), t-butyl 2-bromopropionate (22 g) and triethylamine (12.7 g) were dissolved in ethyl acetate (150 ml), and stirred and heated under reflux for 48 hr, under an atmosphere of nitrogen. Methylene chloride (300 ml) was added to the cooled solution: the mixture was thoroughly washed with sodium hydroxide solution (10% w/w, 300 ml), water (200 ml) and brine; and dried (MgSO4). The solvent was evaporated and the residual oil triturated with hexane (2x200 ml) to give t-butyl (triphenylphosphoranylidene)propionate (33 g, 67%) as a yellow powder; mp 144°-151° C.; partial NMR (250 MHz, CDCl3): 1.0(br signal, 9H, t-butyl), 1.55(d, J=14.4 Hz, 3H, CH3), 7.3-7.9(complex m, 15H, ArH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041460
Source datasetuspto-grants-1991_08
ORD IDord-2fd676c621494c22be734f00bf75f18e
Source noteuspto-grants-1991_08