HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450439Generated: October 29, 2026
Dimethyl Sulfoxide → HCID 18930351, compound
https://huagongshe.com/reaction/1450439
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 18930330 | HCID 18930330 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18930351 | HCID 18930351 | — |
Reaction Steps
Dissolve oxalyl chloride (1.23 g, 9.67 mmol) in methylene chloride (100 mL), place under an argon atmosphere and cool to -78° C. Add dimethylsulfoxide (1.43 mL) and stir for 15 minutes. Add, by dropwise addition, a solution of α-[1-(2-phenylethyl)-4-piperidinyl]-2-thiophenemethanol 8.06 mmol) in methylene chloride (100 mL). Stir at -78° C. for 30 minutes, then add triethylamine (6.07 mL). Stir at -78° C. for 30 minutes, remove the ice bath and allow to warm to room temperature. Evaporate the solvent in vacuo and partition between methylene chloride and water. Separate the organic phase and extract the aqueous phase with methylene chloride. Combine the organic phases, wash with water and dry (MgSO4). Evaporate the solvent in vacuo and recrystallize (isopropanol) to give the title compound as a white crystalline solid; mp 77°-79° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05602147 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-7014446f1d274dc39ffb20b712c1dcba |
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| Source note | uspto-grants-1997_02 |
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