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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379143Generated: November 2, 2026

Trifluoroacetic anhydride → 7-Methoxy-1H-isothiochromen-4(3H)-one

https://huagongshe.com/reaction/1379143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantSodium CarbonateHCID 10340—
Reactant2-[(3-Methoxyphenyl)methylsulfanyl]acetic acidHCID 323071—
SolventTrifluoroacetic acidHCID 6422—
Product7-Methoxy-1H-isothiochromen-4(3H)-oneHCID 32325549%

Reaction Steps

3-methoxybenzylmercaptoacetic acid from Step 2 (10.82 g) was dissolved in trifluoroacetic acid (50 mL). Trifluoroacetic acid anhydride (25 mL) was added and the reaction stirred under a nitrogen atmosphere for 0.25 hours. At this time, TLC showed no starting material. The solution was carefully poured into 10% Na2CO3 solution (500 mL) which was stirring vigorously. The organics were extracted into ether (500 mL) and washed with brine (300 mL), dried over MgSO4 and concentrated in vacuo. The resulting brown solid was purified by silica gel chromatography eluting with 20% ethyl acetate in hexane to yield 7-methoxyisothiochroman-4-one (4.84 g, 49%): 1H NMR (CDCl3) δ=3.48p (t, 2H, J=0.8 Hz), 3.83p (s, 3H), 3.84p (s, 2H), 6.6p (d, 1H, J=2.4 Hz), 6.83p (dd, 1H, J=2.4, 8.9 Hz), 8.0p (d, 1H, J=8.9 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670532
Source datasetuspto-grants-1997_09
ORD IDord-48dd472730bd4996b919988bb3326303
Source noteuspto-grants-1997_09