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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 741764Generated: October 30, 2026

Methanol → HCID 15294981, compound

https://huagongshe.com/reaction/741764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPyridineHCID 1049—
ReactantChloroformHCID 6212—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 9982581HCID 9982581—
ProductHCID 15294981HCID 15294981—

Reaction Steps

A mixture of 10 mg of (6-hydroxy-2-(4-hydroxycyclohexyl)benzo[b]thien-3-yl][4-[2-(1-piperidinyl)ethoxy]phenyl]methanone, 0.5 mL of acetic anhydride, and 0.5 mL of pyridine is agitated for 18 hours at room temperature. Ice is added to the reaction mixture, and the system is agitated for 30 minutes, after which the organic layer is extracted with ethyl acetate, washed with water and a saturated aqueous solution of sodium hydrogencarbonate, and dried with anhydrous magnesium sulfate. The solvent is distilled off, and the crude product thus obtained is refined by TLC (developing solvent was chloroform:methanol=9:1), which gives 5 mg of [6-acetoxy-2-(4-acetoxycyclohexyl)benzo[b]thien-3-yl][4-[2-(1-piperidinyl)ethoxy]phenyl]methanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552433
Source datasetuspto-grants-1996_09
ORD IDord-5f8fcd35a89d4b2aa2cc136fffca999c
Source noteuspto-grants-1996_09