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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69085Generated: October 25, 2026

Trifluoroacetic acid → Benzyl 1,2-dihydrospiro[indole-3,4'-piperidine]-1'-carboxylate

https://huagongshe.com/reaction/69085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPhenylhydrazineHCID 7516—
ReactantBenzyl 4-formylpiperidine-1-carboxylateHCID 2776272—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventAcetonitrile tolueneHCID 21584213—
ProductBenzyl 1,2-dihydrospiro[indole-3,4'-piperidine]-1'-carboxylateHCID 1091425634.1%

Reaction Conditions

Temperature35 °C

Reaction Steps

A solution of phenyl hydrazine (1.29 g, 12.0 mmol) and trifluoroacetic acid (3.0 mL) in a 49/1 solution of toluene/acetonitrile (50 mL) is heated at 35° C. 4-Formyl-piperidine-1-carboxylic acid benzyl ester (2.7 g, 10.91 mmol) is dissolved in a 49/1 solution of toluene/acetonitrile (10 mL) and added dropwise to the mixture (WO2005046682). The mixture is stirred at 35° C. overnight. The resulting solution is cooled to 0° C., and methanol (5 mL) is added. NaBH4 (0.619 g, 16.38 mmol) is added slowly to the solution and the mixture is stirred for 45 min. The mixture is washed with aqueous NH4OH (6%, 25 mL) and brine (30 mL), dried over sodium sulfate, and evaporated to dryness to give a yellow solid. The crude solid is recrystallised from EtOAc to give a pale yellow solid (1.25 g, 1st crop). The mother liquor is evaporated and purified by flash chromatography, eluting with hexane:ethyl acetate (8:2) to give the title compound as a pale yellow solid (1.2 g, 2nd crop) with a total yield (2.4 g, 84%). ESI/MS m/z 323 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822486B2
Source datasetuspto-grants-2014_09
ORD IDord-8322717fa1d54262ad32cb901b3a5e2b
Source noteuspto-grants-2014_09