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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581778Generated: October 31, 2026

Trifluoroacetic acid → HCID 54133431, compound

https://huagongshe.com/reaction/581778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 53821831HCID 53821831—
ProductHCID 54133431HCID 5413343170.7%

Reaction Steps

Trifluoroacetic acid (3 ml) was added to ethyl 4-[N-tert-butoxycarbonyl-N-(2-methoxyethyl)amino]cinnamate (932 mg) in ice water bath and stirred for 15 minutes at same temperature. The solvent was evaporated under reduced pressure. The residue was partitioned between ethyl acetate and aqueous sodium bicarbonate solution. The organic layer was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel eluting to a mixture of n-hexane and ethyl acetate (3:1) and recrystallized from a mixture of n-hexane and ethyl acetate to give ethyl 4-(2-methoxyethylamino)cinnamate (470 mg) as crystals. mp: 49.9-53.4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922711
Source datasetuspto-grants-1999_07
ORD IDord-96567c31123e450d9a155cc4cacd6f71
Source noteuspto-grants-1999_07