HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366171Generated: October 27, 2026
Dimethyl Sulfoxide → tert-butyl N-(2-methyl-4-oxobutan-2-yl)carbamate
https://huagongshe.com/reaction/366171
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | tert-Butyl (4-hydroxy-2-methylbutan-2-yl)carbamate | HCID 15473340 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-butyl N-(2-methyl-4-oxobutan-2-yl)carbamate | HCID 11788901 | 63.6% |
Reaction Steps
DMSO (1.22 mL, 17.2 mmol) was added to a solution of oxalyl chloride (1.1 mL, 12.9 mmol) at -78° C. in dichloromethane (15 mL). The mixture was stirred for 15 min at -78° C. A solution of 3-hydroxy-1,1-dimethylpropylcarbamic acid tert-butyl ester (1.75 g, 8.6 mmol) in dichloromethane (10 mL) was added dropwise over a period of 15 min. The solution was stirred at -78° C. for another 15 min. Triethylamine (6.0 mL, 43 mmol) was added. The solution was stirred at -78° C. for 5 min and then warmed to room temperature. The solution was diluted with dichloromethane (100 mL) and extracted with 1N hydrochloric acid (100 mL). The aqueous phase was extracted with dichloromethane (50 mL). The combined organic layers were washed with saturated sodium hydrogen carbonate solution (100 mL) and dried over magnesium sulfate. The solvent was removed in vacuo. The crude product was purified by column chromatography on silica (140 g) with ethyl acetate/heptane (1:3) to give 1.10 g of 3-(tert-butoxycarbonylamino)-3-methylbutanal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06127391 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-e45dbaf1087544acb3c41192da0bfd26 |
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| Source note | uspto-grants-2000_10 |
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