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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744741Generated: October 30, 2026

Trifluoroacetic acid → HCID 58606962, compound

https://huagongshe.com/reaction/1744741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58606960HCID 58606960—
SolventDichloromethaneHCID 6344—
ProductHCID 58606962HCID 58606962—

Reaction Steps

(S)-(−)-1-(tert-Butoxycarbonyl)-2-azepanecarboxylic acid n-octyl amide (2) (1.00 g; 2.82 mmol) is dissolved in methylene chloride (40 mL) at ambient temperature. Trifluoroacetic acid (20 mL) is added and the solution is stirred for 7 hours at ambient temperature. The solution is concentrated in vacuo at 40° C. The residue is dissolved in methylene chloride (200 mL) and poured onto saturated sodium bicarbonate solution. The pH is adjusted to 9 with saturated potassium carbonate solution. The mixture is shaken and the layers separated. The water layer is extracted with methylene chloride (3 times, 50 mL each). The combined organic extracts are washed with water, dried over MgSO4, filtered, and concentrated in vacuo affording the desired product (3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07018642B2
Source datasetuspto-grants-2006_03
ORD IDord-ea9046cf3e4f4e418fbdb392ea459bfe
Source noteuspto-grants-2006_03