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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987943Generated: October 30, 2026

2,2,2-Trifluoroethanol → HCID 513929, compound

https://huagongshe.com/reaction/987943

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantHCID 513930HCID 513930—
ReactantDi(succinimido) carbonateHCID 676246—
ReactantHCID 85873330HCID 85873330—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
SolventPotassium CarbonateHCID 11430—
ProductHCID 513929HCID 513929—

Reaction Steps

To a stirred solution of (2S,4S)-2-amino-N-{4-[(4-amino-benzenesulfonyl)-isobutyl-amino]-5-hydroxy-pentyl}-3-naphthalen-1-yl-propionamide (0.09 g, 0.17 mmol, product of example 8) in K2CO3 1M (3 mL) and THF (1 mL) was added carbonic acid 2,5-dioxo-pyrrolidin-1-yl ester 2,2,2-trifluoroethyl ester (0.05 g, 0.20 mmol), prepared from 2,2,2-trifluoroethanol, N,N′-disuccinimidyl carbonate and triethylamine in tetrahydrofuran. The mixture was stirred to room temperature for 24 h. Ethyl acetate was added and the organic layer was washed with water, then dried with MgSO4 and concentrated. The residue was purified by flash chromatography eluting with a mixture of hexane/EtOAc. The yield obtained was 10%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06632816B1
Source datasetuspto-grants-2003_10
ORD IDord-b1446caa3194486b8ed22a52c23c1357
Source noteuspto-grants-2003_10