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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514163Generated: November 1, 2026

Trifluoroacetic acid → HCID 86691576, compound

https://huagongshe.com/reaction/514163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86691577HCID 86691577—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86691576HCID 86691576—

Reaction Steps

A solution of ethyl 2-tert-butoxy-2-(3-methyl-1-(trifluoromethylsulfonyloxy)naphthalen-2-yl)acetate (6.0 grams, ˜13 mmol, semipure) in DCM (60 mL) was treated with TFA (6.0 mL) at 23° C. The reaction was diluted with H2O (60 mL) and the organic phase collected. The aqueous layer was extracted with DCM (2×30 mL). The combined organic layers were dried (Na2SO4), filtered, and concentrated. The residue (5.5 grams) was used in the next reaction without further purification. 1H NMR (400 MHz, CDCl3): δ 8.08-8.06 (m, 1H), 7.81-7.78 (m, 1H), 7.69 (s, 1H), 7.62-7.55 (m, 2H), 5.81 (app. s, 1H), 4.35-4.21 (m, 2H), 3.26 (app. s, broad, 1H), 2.50 (s, 3H), 1.21 (t, J=7.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102614B2
Source datasetuspto-grants-2015_08
ORD IDord-63f8c00c623048e6b892a369b3b94bea
Source noteuspto-grants-2015_08