HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338994Generated: October 30, 2026
tert-Butanol → Tert-butyl (2-fluoro-3-methoxyphenyl)carbamate
https://huagongshe.com/reaction/338994
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 2-Fluoro-3-methoxybenzoic acid | HCID 3390679 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tert-butyl (2-fluoro-3-methoxyphenyl)carbamate | HCID 44203148 | 64% |
Reaction Steps
A solution of 2-fluoro-3-methoxybenzoic acid (2.50 g, 14.69 mmol) and DIEA (3.07 mL, 17.63 mmol) in a mixture of toluene (12 mL) and t-BuOH (12 mL) was stirred over 4 Å molecular sieves (3 g) for 1 hour at ambient temperature, followed by addition of diphenyl phosphoryl azide (3.9 mL, 17.63 mmol) and the mixture heated at reflux for 18 hours. The cooled reaction mixture was filtered and the filtrate concentrated under reduced pressure. The residue was dissolved in ethyl acetate (50 mL) and washed with 1N HCl solution, saturated sodium bicarbonate solution, water and brine, then dried (MgSO4), filtered and concentrated under reduced pressure. The residue was purified by column chromatography (Biotage 40M; 2.5% ethyl acetate/hexanes) to afford tert-butyl 2-fluoro-3-methoxyphenylcarbamate (2.27 g, 64% Yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889704B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-7bce5b49414c4957a4d104e56ae42b26 |
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| Source note | uspto-grants-2014_11 |
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