HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171766Generated: November 3, 2026
Dimethyl Sulfoxide → 1-Boc-piperidine-3-carboxaldehyde
https://huagongshe.com/reaction/1171766
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | tert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylate | HCID 2763851 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Boc-piperidine-3-carboxaldehyde | HCID 9964448 | 93.8% |
Reaction Steps
DMSO (0.18 mL, 2.6 mmol) in CH2Cl2 (5 mL) was added dropwise to a solution of oxalyl chloride (2M in CH2Cl2, 0.65 mL, 1.3 mmol) in CH2Cl2 (4 mL) at −78° C. The resulting mixture was stirred at −68° C. for 15 minutes. 3-Hydroxymethyl-piperidine-1-carboxylic acid tert-butyl ester (Dean A. Wacker et al. Bioorganic & Medicinal Chemistry Letters 2002, 12, 1785-1789) (0.22 g, 1.0 mmol) in CH2Cl2 (4 mL) was added dropwise and after 15 min stirring at −78° C., Et3N (6 mL) was added. The resulting solution was stirred at ambient temperature for 16 h. Water was added and the mixture was extracted with diethyl ether, the organic layer was dried (Na2SO4) and concentrated to give the product as an yellow oil (0.20 g, 92% yield). This crude product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07829707B2 |
|---|
| Source dataset | uspto-grants-2010_11 |
|---|
| ORD ID | ord-5c06e1106b2f4d9e820ad4fe73bdedfa |
|---|
| Source note | uspto-grants-2010_11 |
|---|