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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870354Generated: November 4, 2026

Trifluoroacetic acid → HCID 11718248, compound

https://huagongshe.com/reaction/870354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 68912510HCID 68912510—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 11718248HCID 1171824850.2%

Reaction Steps

Allyl-{(S)-6-[(4-isopropyl-benzenesulfonyl)-methyl-amino]-1,2,3,4-tetrahydronaphthalen-2-yl}-carbamic acid tert-butyl ester (672 mg, 1.35 mmol) was dissolved in dichloromethane (30 ml). Trifluoroacetic acid (1 ml) was added and the reaction mixture was stirred at room temperature overnight. The reaction mixture was evaporated to dryness. Ethyl acetate (100 ml) was added and extracted with NaOH (2M). The organic layer was dried over magnesium sulfate, filtered, and evaporated to dryness to yield 1.05 g of crude product. The crude product was dissolved in ethyl acetate (20 ml) and the precipitate was collected to yield the desired compound (270 mg, 50%). The mother liquid was reduced in vacuo to yield an oil (840 mg, 54% purity).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969552B2
Source datasetuspto-grants-2015_03
ORD IDord-a6c4d510fbf64df28aab6537e8c77990
Source noteuspto-grants-2015_03