HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41014Generated: October 28, 2026
Dimethyl Sulfoxide → tert-butyl N-((1-formylcyclopentyl)methyl)carbamate
https://huagongshe.com/reaction/41014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | tert-butyl N-{[1-(hydroxymethyl)cyclopentyl]methyl}carbamate | HCID 57478044 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-butyl N-((1-formylcyclopentyl)methyl)carbamate | HCID 57480691 | 94% |
Reaction Steps
To a solution of oxalyl chloride (456 μL, 5.38 mmol) in DCM (30.0 mL) at −78° C. was added DMSO (637 μL, 8.97 mmol) and the resulting mixture was stirred for 5 minutes. tert-Butyl [1-(hydroxymethyl)cyclopentyl]methylcarbamate (1.03 g, 4.48 mmol) in DCM (10.0 mL) was added and the resulting mixture was stirred for 30 minutes at −78° C. TEA (2.50 mL, 17.9 mmol) was added and the resulting mixture was allowed to warm to ambient temperature over 30 minutes. Water was added. The organic phase was washed sequentially with 0.1 N HCl, water, saturated sodium bicarbonate solution, and brine, and then dried over sodium sulfate and the solvent was removed in vacuo to afford the product (957 mg, 94%). 1H NMR (300 MHz, CDCl3): δ□ 9.39 (s, 1H), 4.94 (br s, 1H), 3.25 (d, 2H), 1.89-1.46 (m, 8H), 1.41 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530485B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-8d212026231a4663a14138247da8e777 |
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| Source note | uspto-grants-2013_09 |
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