HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430686Generated: October 29, 2026
Dimethyl Sulfoxide → N-p-toluoyl valinaldehyde
https://huagongshe.com/reaction/430686
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | N-p-toluoyl valinol | HCID 18346087 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-p-toluoyl valinaldehyde | HCID 53763109 | 56.6% |
Reaction Steps
Dimethylsulfoxide (2.2 ml, 31 mmol ) was slowly added via syringe to a stirred−78° C. solution of oxalyl chloride (15 ml, 171 mmol) in methylene chloride (35 ml) under inert atmosphere. After 10 min., a solution of N-p-toluoyl valinol (6.0 g, 29 mmol) in methylene chloride (50 ml) was added and the stirring was continued for additional 15 min. Triethylarine was added (6 ml, 389 mmol) and the reaction was allowed to warm to ambient temperature. After 1.5 h, the reaction was diluted with 50% ethyl acetate in hexanes and washed with water and brine. Filtration through a pad of silica gel and subsequent solvent removal left a solid residue. Chromatography eluting with 20% ethyl acetate in hexanes, then 33% ethyl acetate in hexanes gave N-p-toluoyl valinaldehyde (3.6 g) as a solid, which was utilized in Step 6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06323223B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-4b177b81136249ada65d81d1d3b105c4 |
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| Source note | uspto-grants-2001_11 |
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