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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990506Generated: October 31, 2026

Acetic Acid → 3-[[[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]methyl]amino]phenol

https://huagongshe.com/reaction/990506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-AminophenolHCID 11568—
ReactantBenzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)-HCID 118803—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
Product3-[[[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]methyl]amino]phenolHCID 1095801678%

Reaction Steps

To a solution of 3-aminophenol (4.91 g, 45.0 mmol) and 3-(1,1,2,2-tetrafluoroethoxy)benzaldehyde (10.0 g, 45.0 mmol) dissolved in 100 mL of 1,2-dichloroethane was added sodium triacetoxyborohydride (14.28 g 67.5 mmol) and glacial acetic acid (2.7 mL, 47.3 mmol). The reaction mixture was stirred for 6 h, water was added, and the mixture was extracted with dichloromethane. The organics were washed with saturated aqueous sodium bicarbonate then dried over MgSO4. The dried organic layer was evaporated to give 11.00 g (78%) of the desired 3-[[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]phenol product as a dark orange oil. 1H NMR(CDCl3) δ4.32 (s, 2H), 5.88 (tt, 1H), 6.08 (t, 1H), 6.17-6.22 (m, 2H), 7.00 (t, 1H), 7.11 (dd, 1H), 7.24-7.27 (m, 2H), 7.33 (t, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458852B1
Source datasetuspto-grants-2002_10
ORD IDord-26f820672f2347a3a587fecea77dcd28
Source noteuspto-grants-2002_10