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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017023Generated: November 1, 2026

Acetic Acid → HCID 18407223, compound

https://huagongshe.com/reaction/1017023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant3-(Trifluoromethoxy)benzaldehydeHCID 605139—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-[(3-Bromophenyl)amino]-1,1,1-trifluoro2-propanolHCID 23506102—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 18407223HCID 18407223119.2%

Reaction Steps

EX-633B) The 3-[(3-bromophenyl)amino]-1,1,1-trifluoro-2-propanol (1.14 g, 4 mmol) from EX-633A and 3-(trifluoromethoxy)benzaldehyde (0.78 g, 4.1 mmol) were dissolved in dichloroethane (18 mL). Acetic acid (0.253 mL, 4.2 mmol) and solid NaBH(OAc)3 (1.07 g, 5.05 mmol) were added. The mixture was stirred at room temperature for 3 h. then acidified with 1 N HCl solution. After neutralizing to pH 7.5 with 2.5 N sodium hydroxide, the mixture was extracted with methylene chloride. The organic layer was washed with brine and water, then dried over anhydrous MgSO4, and evaporated to give 1.12 g (62%) of the desired N-3-bromophenyl-[[[3-(trifluoromethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol product as a brown oil, which was greater than 80% pure by reverse phase HPLC analysis. HRMS calcd. for C17H14NO2F6Br 458.0190 [M+H]+, found: 458.0199.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476057B1
Source datasetuspto-grants-2002_11
ORD IDord-3240cc2589a7437295e0cf47d765f95a
Source noteuspto-grants-2002_11