HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098352Generated: October 30, 2026
Dimethyl Sulfoxide → Methyl 4-formylpiperidine-1-carboxylate
https://huagongshe.com/reaction/1098352
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Methyl 4-(hydroxymethyl)piperidine-1-carboxylate | HCID 45123042 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-formylpiperidine-1-carboxylate | HCID 45123041 | 78% |
Reaction Steps
To a solution of oxalyl chloride (4.1 mL, 8.2 mmol) in dichloromethane (4 mL) at −78° C. was added dropwise a solution of dimethylsulfoxide (1.2 mL, 16.4 mmol) in dichloromethane (4 mL). After stirring for 5 min, a solution of 4-hydroxymethyl-piperidine-1-carboxylic acid methyl ester (1.3 g, 7.5 mmol) in dichloromethane (5 mL) was added. The resulting solution was stirred for another 5 min, then triethylamine (5.2 mL, 37.3 mmol) was added and the mixture allowed to warm to −10° C. After stirring for 1 h, dichloromethane (100 mL) was added, and the organic layer was washed with 1M aqueous phosphoric acid, 1M aqueous sodium hydroxide, and brine. The solution was dried over sodium sulfate then evaporated to afford the title intermediate as a wheat colored oil (1.0 g, 5.8 mmol, 78%). 1H NMR (300 MHz, DMSO-d6): δ (ppm) 1.36 (m, 2H), 1.83 (m, 2H), 2.48 (br m, 1H), 2.93 (br t, 2H), 3.56 (s, 3H), 3.80 (br d, 2H), 9.56 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143279B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-a4a6b0167e2349cab102b2401a0997f6 |
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| Source note | uspto-grants-2012_03 |
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