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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646525Generated: October 30, 2026

Water → HCID 86608638, compound

https://huagongshe.com/reaction/646525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantEthoxalyl chlorideHCID 20884—
ReactantHCID 86608637HCID 86608637—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTolueneHCID 1140—
ProductHCID 86608638HCID 86608638—

Reaction Steps

To a solution of 1-(2-Benzyloxy-5-chloro-phenyl)-2-(triphenyl-λ5-phosphanylidene)-ethanone (0.49 g, 0.94 mmol), NEt3 (96 mg, 0.94 mmol) and DMAP (12 mg, 0.09 mmol) in dry toluene (20 ml) at room temperature, ethyl chlorooxoacetate (0.38 g, 2.78 mmol) in toluene (5 ml) was added. The mixture was stirred for 2 hours and poured into water (50 ml). The organic layer was separated and the aq. layer was extracted with EtOAc (2×40 ml). The combined organic layers were then washed with sat. NaHCO3 solution (2×40 ml), sat. citric acid (1×40 ml), brine (1×40 ml) and dried. Crude oil (0.36 g) was purified by chromatography, eluted with EtOAc. Rf=0.88. 1H NMR (d6-acetone) δ=7.75-7.40 (15H, m); 7.30 (1H, dd); 7.15 (1H, d); 7.05 (1H, d); 5.10 (2H, s); 3.60 (2H, q) and 1.10 (3H, s). LCMS: (M+1)+=621.2 (RT=6.49 min.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705027B2
Source datasetuspto-grants-2010_04
ORD IDord-0828d980d4ca449182de6e2c8d62a077
Source noteuspto-grants-2010_04