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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481773Generated: October 30, 2026

Trifluoroacetic acid → HCID 19067141, compound

https://huagongshe.com/reaction/481773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 19067143HCID 19067143—
SolventDichloromethaneHCID 6344—
ProductHCID 19067141HCID 1906714165%

Reaction Steps

1.11 g of N-benzyloxycarbonyl-4-tert-butoxycarbonylmethyloxy-2,6-dimethylpiperidine was dissolved in 5 ml of methylene chloride, and 2 ml of trifluoroacetic acid was added. The solution was stirred overnight at room temperature, and the resulting solution was concentrated under reduced pressure. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography. From the fractions eluted with chloroform-methanol (9:1 v/v) was obtained 0.61 g of N-benzyloxycarbonyl-4-carboxymethyloxy-2,6-dimethylpiperidine, which was an oily product with no color (yield: 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789595
Source datasetuspto-grants-1998_08
ORD IDord-d3466d0402c64911a564a5a53fd18566
Source noteuspto-grants-1998_08