HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643577Generated: October 30, 2026
Trifluoroacetic acid → HCID 11694142, compound
https://huagongshe.com/reaction/643577
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | tert-Butyl carbamate | HCID 77922 | — |
| Reactant | 2-Hydroxy-5-(trifluoromethoxy)benzaldehyde | HCID 1268058 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11694142 | HCID 11694142 | — |
Reaction Steps
A solution of 5-(trifluoromethoxy)salicylaldehyde (4.85 mmol, 1.0 g), tert-butyl carbamate (14.55 mmol, 1.70 g), triethylsilane (14.55 mmol, 2.3 mL), trifluoroacetic acid (9.7 mmol, 0.72 mL) in acetonitrile was stirred at room temperature overnight. The reaction was quenched with saturated NaHCO3 and extracted with EtOAc. The combined organic layers were dried over Na2SO4 and purified by silica gel chromatography (15%-100% EtOAc/hexane). The resulting yellow solid was then dissolved in a mixture of TFA (10 mL) and dichloromethane (20 mL) and stirred for 2 hours at room temperature. The volatile solvents were then removed by rotovap to afford 2-(aminomethyl)-4-(trifluoromethoxy)phenol as a yellow oil. 1H NMR (CD3OD) 7.28 (s, 1H), 7.22 (m, 1H), 6.97 (m, 1H), 4.13 (s, 2H), 1.59 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700591B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-8455746be98448b09a0da6c48299ad3d |
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| Source note | uspto-grants-2010_04 |
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