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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825704Generated: October 27, 2026

6-Aminohexanoic Acid → 6-(Trifluoroacetamido)hexanoic Acid

https://huagongshe.com/reaction/1825704

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Aminohexanoic AcidHCID 564—
ReactantTriethylamineHCID 8471—
ReactantEthyl trifluoroacetateHCID 9794—
SolventMethanolHCID 887—
Product6-(Trifluoroacetamido)hexanoic AcidHCID 30359384%

Reaction Steps

6-Aminocaproic acid (1, 6.55 g, 50 mmol) was suspended in methanol (30 ml) and treated with triethylamine (6.9 ml, 100 mmol) followed by ethyl trifluoroacetate (7.2 ml, 60 mmol). The mixture was stirred at room temperature (r.t.) during 40 hours. The unreacted solid precipitate was filtered, the filtrate was evaporated in vacuo and crystallized from benzene-hexane mixture. Trifluoroacetyl derivative (2) had an 84% yield (9.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049073B2
Source datasetuspto-grants-2006_05
ORD IDord-fc39e95fb3e3414984008ccc023857ab
Source noteuspto-grants-2006_05