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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519622Generated: November 2, 2026

Sodium cyanoborohydride → HCID 86694485, compound

https://huagongshe.com/reaction/1519622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantTert-butyl 3-(trifluoromethyl)piperazine-1-carboxylateHCID 66599850—
Reactant2-(Methyloxy)-4-(2-oxoethyl)benzonitrileHCID 77231259—
SolventMethanolHCID 887—
ProductHCID 86694485HCID 86694485—

Reaction Steps

To a mixture of tert-butyl 3-(trifluoromethyl)piperazine-1-carboxylate (72 mg, 0.28 mmol) and 2-methoxy-4-(2-oxoethyl)benzonitrile (50 mg, 0.28 mmol) in methanol (2.5 mL) at 0° C. was added sodium cyanoborohydride (25 mg, 0.40 mmol) and the mixture was stirred at room temperature for 12 hours. The reaction mixture was concentrated and purified by column chromatography (4->30% ethyl acetate:hexanes) to provide tert-butyl 4-[2-(4-cyano-3-methoxyphenyl)ethyl]-3-(trifluoromethyl)piperazine-1-carboxylate. LC-MS (IE, m/z): 414.4 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073882B2
Source datasetuspto-grants-2015_07
ORD IDord-89aeaa4b2d56484db6fda6151953444d
Source noteuspto-grants-2015_07