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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926150Generated: November 1, 2026

Water → Ethyl 2-(7-bromo-3-methyl-1-(trifluoromethylsulfonyloxy)naphthalen-2-yl)-2-oxoacetate

https://huagongshe.com/reaction/926150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium DithioniteHCID 24489—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantEthyl 2-(7-bromo-3-methyl-1-(trifluoromethylsulfonyloxy)-naphthalen-2-yl)-2-hydroxyacetateHCID 87279267—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-(7-bromo-3-methyl-1-(trifluoromethylsulfonyloxy)naphthalen-2-yl)-2-oxoacetateHCID 86691550—

Reaction Steps

To a solution of ethyl 2-(7-bromo-3-methyl-1-(trifluoromethylsulfonyloxy)naphthalen-2-yl)-2-hydroxyacetate (˜8.7 mmol) in CH2Cl2 (40 mL) was added Dess-Martin periodinane (4.07 g, 9.6 mmol). After 1.5 h, a saturated solution of Na2S2O4 (20 mL) and water (20 mL) was added. The mixture was stirred vigorously for 30 min. The layers were separated, and the organic layer was dried, filtered, and concentrated in vacuo. The crude material was purified by column chromatography (EtOAc/hexanes) to give 3 the titled compound. 1H-NMR: 400 MHz, (CDCl3) δ: 8.22 (s, 1H), 7.70 (m, 3H), 4.41 (q, J=7 Hz, 2H), 2.47 (s, 3H), 1.39 (t, J=7 Hz, 3H). 19F-NMR: 377 MHz, (CDCl3) δ: −73.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284323B2
Source datasetuspto-grants-2016_03
ORD IDord-af842949535a4317850dc220c5336849
Source noteuspto-grants-2016_03