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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399634Generated: October 26, 2026

Methanol → HCID 18967835, compound

https://huagongshe.com/reaction/399634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant3-(Chloromethyl)benzoyl chlorideHCID 2733324—
ReactantHCID 15291611HCID 15291611—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 18967835HCID 1896783581%

Reaction Steps

0.6 ml of 3-chloromethylbenzoyl chloride is added dropwise, at 0° C., to 1.6 g of the compound of Example 4 dissolved in 10 ml of anhydrous pyridine. After 2 hours at 0° C., methanol is added to hydrolyze the excess acid chloride and the organic phase is diluted with methylene chloride. This is then washed with 2N hydrochloric acid, with saturated aqueous sodium bicarbonate and then with saturated aqueous sodium chloride and dried over anhydrous sodium sulphate. The organic solvent is evaporated off and the product is purified on a column of silica, using a mixture of cyclohexane and ethyl acetate (20:1 v/v) as eluent, to give the expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05821255
Source datasetuspto-grants-1998_10
ORD IDord-c3abf37985a04eedbdaced9381a9dde5
Source noteuspto-grants-1998_10