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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882796Generated: November 1, 2026

Ethyl trifluoroacetate → (1R,3S,4S)-3-[(2,2,2-Trifluoro-acetylamino)-methyl]-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/882796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trifluoroacetateHCID 9794—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-butyl (1R,3S,4S)-3-(aminomethyl)-2-azabicyclo[2.2.1]heptane-2-carboxylateHCID 66866957—
SolventTetrahydrofuranHCID 8028—
Product(1R,3S,4S)-3-[(2,2,2-Trifluoro-acetylamino)-methyl]-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl esterHCID 86649700—

Reaction Steps

Ethyl trifluoroacetate (12.2 mmol, 1.30 eq) is added to a solution of (1R,3S,4S)-3-aminomethyl-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester (9.42 mmol, 1.00 eq) and DIPEA (14.1 mmol, 1.50 eq) in THF (25 mL). After 50 min the mixture is concentrated in vacuo, diluted with TBME (100 mL) and washed twice with aq. citric acid (5%) and water respectively. The organic layer is dried over MgSO4 and concentrated in vacuo to give a crude product which is used without further purification. LC-MS (basic): tR=0.95 min; [M+H]+=323.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236801B2
Source datasetuspto-grants-2012_08
ORD IDord-f3b1a520da93430fac43de711a19aa10
Source noteuspto-grants-2012_08