HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405949Generated: October 29, 2026
tert-Butanol → Tert-butyl 5-(trifluoromethyl)thiophen-2-ylcarbamate
https://huagongshe.com/reaction/1405949
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 5-(Trifluoromethyl)thiophene-2-carboxylic acid | HCID 2049051 | — |
| Product | Tert-butyl 5-(trifluoromethyl)thiophen-2-ylcarbamate | HCID 86718387 | — |
Reaction Steps
To 5-(trifluoromethyl)thiophene-2-carboxylic acid in tBuOH (50 mL) was added triethylamine (1.53 mL, 11 mmol) and diphenylphosphoryl azide (DPPA) (2.4 mL, 11 mmol). This mixture was heated to 90° C., and was stirred overnight (ca. 16 hours). Thin layer chromatography (TLC) indicated that the reaction was complete. The solvent was removed under reduced pressure, the residue was dissolved in ethyl acetate (EtOAc) and washed 1× with NaHCO3 aq sat, 1× with citric acid (10% aqueous), and 1× brine. The solution was dried over MgSO4, filtered and concentrated. After silica gel chromatography (5 to 20% EtOAc/hexanes) the title compound was afforded (1.46 g, 44% over 3 steps) as a yellow/orange solid, mp 118-120° C.; Rf=0.31 (10% EtOAc/hex); 1H NMR (DMSO-d6) δ 11.03 (br s, 1H), 7.38 (app d, 1H, J=4.1 Hz), 6.51 (app d, 1H, J=3.3 Hz), 1.49 (s, 9H); GCMS (EI) m/z 267 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916578B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-e0cedbe773804b7d8681e3262682aa2f |
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| Source note | uspto-grants-2014_12 |
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