HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843266Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 22617036, compound
https://huagongshe.com/reaction/843266
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1-Methyl-3-hydroxymethyl-4-(3,4-dichlorophenyl)piperidine | HCID 10401105 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22617036 | HCID 22617036 | 111.3% |
Reaction Steps
To a solution of oxalyl chloride (3.3 mL, 37.9 mmol) in methylene chloride (100 mL) cooled below −40° C. was added dimethyl sulfoxide (5.6 mL, 79 mmol) in methylene chloride (5 mL). The reaction was stirred for another 30 min at −40° C. and 1-methyl-3-hydroxymethyl-4-(3,4-dichlorophenyl)piperidine (9.0 g, 33 mmol) in methylene chloride (100 mL) was added over 15 min while keeping the temperature below −40° C. The reaction was stirred for another 30 min at this temperature and then allowed to heat to room temperature. Water (100 mL) was added and the organic phase separated off. The aqueous phase was extracted with methylene chloride (2×100 mL). The combined organic extracts were dried over magnesium sulphate and evaporated to dryness to give 10 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06376673B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-2e261140127c4ce491582d9179832ccc |
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| Source note | uspto-grants-2002_04 |
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