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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007856Generated: October 26, 2026

Ethanol → 6-Hydroxy-2-(4-hydroxyphenyl)-3-(4-(2-piperidinoethoxy)-benzoyl]benzo[b]thiophene Hydrochloride 1,2-Dichloroethane

https://huagongshe.com/reaction/1007856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethanolHCID 887—
ReactantBoron TrichlorideHCID 25135—
ReactantRaloxifene Bismethyl Ether (hydrochloride)HCID 45260096—
Solvent1,2-DichloroethaneHCID 11—
Product6-Hydroxy-2-(4-hydroxyphenyl)-3-(4-(2-piperidinoethoxy)-benzoyl]benzo[b]thiophene Hydrochloride 1,2-DichloroethaneHCID 9916879—

Reaction Conditions

Temperature35 °C

Reaction Steps

A solution of 6-methoxy-2-(4-methoxyphenyl)-3-(4-(2-piperidinoethoxy)benzoyl]benzo[b]thiophene hydrochloride (2.0 g) in 1,2-dichloroethane (20 mL) was treated with boron trichloride (2.0 mL). The resulting mixture was stirred at 35° C. for about 18 hours. A mixture of ethanol and methanol (10 mL, 95:5, 3A) was treated with the reaction mixture from above, causing the alcoholic mixture to reflux. Upon complete addition, the resulting crystalline slurry was stirred at 25° C. After one hour, the crystalline product was filtered, washed with cold ethanol (10 mL), and dried at 40° C. in vacuo to give 1.78 g of the title compound. The X-ray powder diffraction pattern is identical to that reported in Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797719B2
Source datasetuspto-grants-2004_09
ORD IDord-86a2d21a65fc4037bd7b088758a92bb1
Source noteuspto-grants-2004_09