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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243499Generated: November 1, 2026

Trifluoroacetic acid → HCID 68543717, compound

https://huagongshe.com/reaction/2243499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 68544784HCID 68544784—
SolventDichloromethaneHCID 6344—
ProductHCID 68543717HCID 68543717—

Reaction Steps

Step H Deprotection: A solution of 7-tert-Butoxycarbonylamino-1-ethoxycarbonylmethoxy-3,8-dithia-cyclopenta[a]indene-2-carboxylic acid methyl ester (170 mg, 0.37 mmol) in DCM (6 mL) was cooled to 0° C. Trifluoroacetic acid (1.2 mL) was then added, and the solution was allowed to warm to ambient temperature, stirring a total of four hours, after which the reaction was judged complete by TLC. The reaction mixture was concentrated in vacuo, dissolved in ethyl acetate, and washed with sodium bicarbonate (3×10 mL). The organic layer was then concentrated in vacuo, affording 7-Amino-1-ethoxycarbonylmethoxy-3,8-dithia-cyclopenta[a]indene-2-carboxylic acid methyl ester in a quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674822B2
Source datasetuspto-grants-2010_03
ORD IDord-25775d23cdfc4069847bfd019f56f67d
Source noteuspto-grants-2010_03