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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109310Generated: November 1, 2026

HCID 10730396, compound → HCID 88451558, compound

https://huagongshe.com/reaction/1109310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10730396HCID 10730396—
Reactantp-Anisyldiphenylmethyl chlorideHCID 14836583—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 88451558HCID 88451558—

Reaction Steps

To a solution of 2.8 grams (10.6 mmol) of N-(2-hydroxy-ethoxy)-4-pivaloylbenzamide in 5 ml of methylene chloride and 3 ml of pyridine at 0° C. are added 3.92 grams (12.7 mmol) of ρ-anisylchlorodiphenylmethane. The mixture is warmed to room temperature over two hours and then diluted with 40 ml of methylene chloride. This solution is washed with 50 ml of 10% sodium bicarbonate and 30 ml of brine, dried over magnesium sulfate and concentrated by evaporation. The residue is purified by column chromatography using 5:1 hexane/ethyl acetate as the eluent to obtain the protected product, N-(2-[ρ-anisyldiphenylmethyloxy]ethoxy)-4-pivaloylbenzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05319123
Source datasetuspto-grants-1994_06
ORD IDord-437201af911d4e7f9519cf0cf8fb770d
Source noteuspto-grants-1994_06