HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598045Generated: October 27, 2026
(Diethylamino)sulfur trifluoride → Tert-butyl (2-fluoro-2-methylpropyl)carbamate
https://huagongshe.com/reaction/598045
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | tert-Butyl 2-hydroxy-2-methylpropylcarbamate | HCID 11106129 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl (2-fluoro-2-methylpropyl)carbamate | HCID 72698934 | 70.9% |
Reaction Steps
A solution of tert-butyl 2-hydroxy-2-methylpropylcarbamate (19.2 g, 101 mmol) in dichloromethane (500 mL) was stirred at −78° C. under a nitrogen atmosphere, and (diethylamino)sulfur trifluoride (DAST)(18.0 g, 112 mmol) was added dropwise. The solution was allowed to warm to room temperature and stirred overnight. Saturated aqueous sodium bicarbonate (150 mL) was added. The organic layer was then separated and washed sequentially with saturated aqueous sodium bicarbonate (150 mL), water (150 mL), and brine (150 mL); dried over magnesium sulfate; filtered; and concentrated under reduced pressure. The resulting oil was purified by automated flash chromatography (FLASH 65I cartridge, eluting with 10% ethyl acetate in hexane) to provide 13.7 g of tert-butyl 2-fluoro-2-methylpropylcarbamate as a light yellow oil that crystallized overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897609B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-7e5ba8712eef419ab41071692cf4dab3 |
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| Source note | uspto-grants-2011_03 |
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