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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902682Generated: October 31, 2026

Water → (2-Chloro-3-trifluoromethyl-benzyl)-(2-thiophen-2-yl-propyl)-amine

https://huagongshe.com/reaction/902682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Chloro-3-(trifluoromethyl)benzylamineHCID 5224207—
Reactant2-(Thiophen-2-yl)propanalHCID 11051743—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
Product(2-Chloro-3-trifluoromethyl-benzyl)-(2-thiophen-2-yl-propyl)-amineHCID 69253724107%

Reaction Steps

To a solution of 2-thiophen-2-yl-propionaldehyde (100 mg, 0.7 mmol) in dry dichloromethane (20 ml) was added 2-chloro-3-trifluoromethyl-benzylamine (30 mg, 0.14 mmol) followed by the addition of sodium triacetoxyborohydride (60.5 mg, 0.28 mmol). After the resulting mixture was stirred at room temperature overnight water was added to quench the reaction. The aqueous layer was extracted with ethyl acetate. The combined organic layers was washed with brine, dried over sodium sulfate and concentrated in vacco. The crude mixture was purified by silica gel column chromatograph using EtOAc:Hexane/25:75 as the eluent to give 50 mg (40% yield) of the title compound as an oil. MS m/e 334.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365085B2
Source datasetuspto-grants-2008_04
ORD IDord-8ee8eb59e042489ea95fc8c016eb9639
Source noteuspto-grants-2008_04