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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105353Generated: November 4, 2026

Trifluoroacetic acid → HCID 68460959, compound

https://huagongshe.com/reaction/2105353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 68461499HCID 68461499—
SolventDichloromethaneHCID 6344—
ProductHCID 68460959HCID 68460959100%

Reaction Steps

The solution of 14.3 g (31.6 mmol) 5-benzyloxy-1-(3-tert-butoxycarbonylamino-propyl)-1H-indole-2-carboxylic acid ethyl ester in 140 mL dichloromethane was cooled to 0° C. and 70 mL (104.2 g, 914 mmol) trifluoroacetic acid was added. The cooling bath was removed and after stirring at room temperature for 1 h, the solution was neutralized with 1M aqueous sodium hydroxide solution and was extracted with dichloromethane. The organic phase was washed with brine, dried over magnesium sulfate, filtered and evaporated to give the crude product as yellow oil (>100%). The compound was pure enough for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579351B2
Source datasetuspto-grants-2009_08
ORD IDord-729535eab356423c87b98cd78869fdad
Source noteuspto-grants-2009_08