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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410421Generated: November 4, 2026

p-Anisoyl chloride → HCID 12521848, compound

https://huagongshe.com/reaction/1410421

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 70670—
ReactantN,O-bis(trimethylsilyl)acetamideHCID 6913588—
SolventDichloromethaneHCID 6344—
ProductHCID 12521848HCID 12521848—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of (carbethoxymethylene)triphenylphosphorane (0.500 g, 1.44 mmol) in DCM (7 ml) under an N2 atmosphere was added N,O-bis(trimethylsilyl)acetamide (0.42 m, 1.7 mmol). The solution was then cooled to 0° C. and p-anisoylchloride (0.250 g, 1.47 mmol) was added. The reaction mixture was then gradually warmed to room temperature and stirred overnight. The reaction was quenched by the addition of H2O (3 ml) and the aqueous phase was extracted with DCM. The combined organic phases were dried over MgSO4 and the solvent removed in vacuo to afford ethyl 3-(4-methoxyphenyl)-3-oxo-2-(triphenylphosphoranylidene)propionate. (0.637 g, 1.32 mmol, 92%) as an off white solid which was used without further purification. 1H NMR (CDCl3) δ 0.62 (3H, t), 3.69 (2H, q), 3.82 (3H, s), 6.86 (2H, d), 7.43-7.55 (9H, m), 7.71-7.80 (8H, m). LCMS (2) Rt: 3.65 min; m/z 483.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921544B2
Source datasetuspto-grants-2014_12
ORD IDord-c3154bc29fa249f6b572cfb4fd000d3c
Source noteuspto-grants-2014_12