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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722228Generated: November 1, 2026

Triphenylphosphine → N-isobutyl acetamidotriphenylphosphonium chloride

https://huagongshe.com/reaction/1722228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-Chloro-N-isobutylacetamideHCID 222359—
SolventBenzeneHCID 241—
ProductN-isobutyl acetamidotriphenylphosphonium chlorideHCID 2304929086%

Reaction Steps

To a solution of triphenylphosphine (229.8 g, 876 mmol) in dry benzene (800 ml) was added N-isobutyl-2-chloroacetamide (131 g, 876 mmol) (prepared by standard methods from 2-chloroacetyl chloride and isobutylamine) in dry benzene (100 ml). The solution was heated under reflux, with vigorous stirring, for 8 hours. Upon cooling, colourless needles formed. These were collected by filtration and the filtrate heated under reflux for a further 8 hours. A second batch of the produce was collected. The combined batches were washed with dry ether and dried in vacuo to give 310 g (86% of theory) of N-isobutyl-acetamidotriphenyl-phosphonium chloride as colourless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855086
Source datasetuspto-grants-1989_08
ORD IDord-976c23b51b7d4feb8549d40691e6e288
Source noteuspto-grants-1989_08