HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243606Generated: November 2, 2026
Dimethyl Sulfoxide → tert-butyl N-methyl-N-(3-oxopropyl)carbamate
https://huagongshe.com/reaction/1243606
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | tert-Butyl (3-hydroxypropyl)methylcarbamate | HCID 10375241 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | tert-butyl N-methyl-N-(3-oxopropyl)carbamate | HCID 10442454 | 100.7% |
Reaction Steps
Dimethylsulfoxide (6.22 ml, 87.6 mmol) was dissolved in dry dichloromethane (100 ml) under nitrogen and the solution was cooled to −78° C. with stirring. Oxalyl chloride (3.95 ml, 45.4 mmol) was then added dropwise and the solution was stirred at −78° C. for a further 30 minutes when effervescence had ceased. A solution of 1,1-dimethylethyl (3-hydroxypropyl)methylcarbamate (6.62 g, 35.0 mmol) in dichloromethane (100 ml) was then added dropwise at −78° C. The resultant solution was stirred at −78° C. for 45 minutes, then a solution of methylamine (24.4 ml, 175 mmol) in dichloromethane (50 ml) was added. The resultant solution was allowed to warm to room temperature and stirred for a further 18 h. The reaction mixture was then poured into brine and extracted with dichloromethane three times. The combined organic fractions were then washed with brine, dried (MgSO4) and evaporated. The residue was triturated with diethyl ether and filtered. The solvent was evaporated to give the title compound (6.60 g, 100%) as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07119109B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-4152c0668aed43b79771701125461947 |
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| Source note | uspto-grants-2006_10 |
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