HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266096Generated: October 25, 2026
Triethylamine → [Benzo[b]thiophene-2-yl][1-(2-phenylethyl)-4-piperidinyl]methanone
https://huagongshe.com/reaction/266096
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | alpha-[1-(2-Phenylethyl)-4-piperidinyl]-2-benzo[b]thiophenemethanol | HCID 18930341 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [Benzo[b]thiophene-2-yl][1-(2-phenylethyl)-4-piperidinyl]methanone | HCID 18930331 | — |
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 (5.42 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 a fluffy white crystalline solid; mp 129°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05650416 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-1f16502ab5d54723934cdff55a1b4da9 |
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| Source note | uspto-grants-1997_07 |
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