Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491693Generated: October 25, 2026

Triethylamine → [Benzo[b]thiophene-2-yl][1-(2-phenylethyl)-4-piperidinyl]methanone

https://huagongshe.com/reaction/1491693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactantalpha-[1-(2-Phenylethyl)-4-piperidinyl]-2-benzo[b]thiophenemethanolHCID 18930341—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
Product[Benzo[b]thiophene-2-yl][1-(2-phenylethyl)-4-piperidinyl]methanoneHCID 18930331—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Dissolve oxalyl chloride (4.22 g, 33.28 mmol) in methylene chloride (200 mL), place under an argon atmosphere and cool to -78° C. Add, by dropwise addition, dimethylsulfoxide (5.4 2 g, 69.33 mmol) and stir at -78° C. for 15 minutes. Add, by dropwise addition, a solution of α-[1-(2-phenylethyl)-4-piperidinyl]-2-benzo[b]thiophenemethanol (9.75 g, 27.73 mmol) in dimethylsulfoxide (150 mL). Stir at -78° C. for 30 minutes, add triethylamine (15.18 g, 0.150 mol) and stir at -78° C. for 1 hour. Remove the ice bath and stir for an additional 1.5 hours. Evaporate the solvent in vacuo and recrystallize (isopropanol) to give the title compound as fluffy white crystalline solid; mp 129°-130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05371093
Source datasetuspto-grants-1994_12
ORD IDord-94f7cb0b49494e3ba17bf44f58b140b8
Source noteuspto-grants-1994_12