HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419084Generated: October 28, 2026
Trifluoroacetic anhydride → HCID 22394204, compound
https://huagongshe.com/reaction/1419084
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | {[(3-Chlorophenyl)methyl]sulfanyl}acetic acid | HCID 2115231 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 22394204 | HCID 22394204 | 51.1% |
Reaction Steps
3-Chlorobenzylmercaptoacetic acid from Step 2 (3.35 g) was dissolved in trifluoroacetic acid (50 mL). Trifluoroacetic acid anhydride (25 mL) was added and the reaction stirred at reflux, under a nitrogen atmosphere for 16 hours. 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 a 0-10% gradient of ethyl acetate in hexane to yield 7-chloroisothiochroman-4-one (1.57 g, 51%): 1H NMR (CDCl3) δ=3.49p (d, 2H, J=0.8 Hz), 3.8p (s, 2H), 7.16p (m, 1H), 7.3p (dd, 1H, J=2.0, 8.4 Hz), 7.96p (d, 1H, J=8.5 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05886016 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-ab67c16ccc72475bb0658cc1ebe88ebc |
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| Source note | uspto-grants-1999_03 |
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