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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226499Generated: October 30, 2026

Ammonia → HCID 15023848, compound

https://huagongshe.com/reaction/2226499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 15023847HCID 15023847—
SolventMethanolHCID 887—
ProductHCID 15023848HCID 15023848—

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 3.95 g (0.011 mole) of 1-t-butoxycarbonyl-3-(2,2,2-trifluoroethoxy)-4-methylsulfonyloxypyrrolidine [prepared as described in step (a) above] and 100 ml of methanol containing 20% w/v ammonia was transferred to an autoclave and then stirred at 140° C. for 10 hours. At the end of this time, the solvent was removed by distillation under reduced pressure, and the residue was mixed with a saturated aqueous solution of sodium carbonate and extracted with ethyl acetate. The organic extract was dried over anhydrous sodium sulfate and concentrated by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel using a 1:9 by volume mixture of ethanol and ethyl acetate as the eluent, to give 1.61 g of 3-amino-1-t-butoxycarbonyl-4-(2,2,2-trifluoroethoxy)pyrrolidine as a colorless oil. Mass Spectrum (CI): m/e 285 (M+ +1), 229 (M+ +1--CH2 =C(CH3)2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05348961
Source datasetuspto-grants-1994_09
ORD IDord-0c24263eec1f4a5ebdc9f0e32613f240
Source noteuspto-grants-1994_09