HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81931Generated: October 26, 2026
(Diethylamino)sulfur trifluoride → Tert-butyl (2-fluoro-2-methylpropyl)carbamate
https://huagongshe.com/reaction/81931
Participants
| Role | Name | HCID | Charge |
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| 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 | 79.4% |
Reaction Steps
A stirred solution of tert-butyl 2-hydroxy-2-methylpropylcarbamate (7.81 g, 41.3 mmol) dissolved in 300 mL of anhydrous CH2Cl2 was cooled to −78° C. under an atmosphere of N2. The reaction mixture was treated with diethylaminosulfur trifloride (DAST) (6.2 mL, 47 mmol) and allowed to warm to ambient temperature overnight. The reaction mixture was treated with saturated NaHCO3 solution and the layers were separated. The organic portion was washed successively with saturated NaHCO3 solution, H2O and brine. The organic portion was dried over Na2SO4, filtered and concentrated under reduced pressure. Chromatography (SiO2, 10% EtOAc/hexanes) gave 6.27 g of tert-butyl 2-fluoro-2-methylpropylcarbamate as an amber oil which solidified on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846710B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-3121fa39df234ee09ca8bb9d34c239bd |
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| Source note | uspto-grants-2014_09 |
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