Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| Reactant | 1-Fluoro-4-(methylthio)benzene | HCID 3083565 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | HCID 10965199 | HCID 10965199 | 58% |
Reaction Steps
A mixture of 4-fluorothioanisole (19c) (4 g, 28.13 mmol), anhydrous aluminium chloride (8.40 g, 63.02 mmol) and carbon disulphide (89 ml) was heated at reflux under argon atmosphere, and acetic arhydride (2.65 ml, 28.07 mmol) was added dropwise in 2 h. After refluxing for 24h, the solution was poured into crushed ice, water (62.48 ml) and concentrated hydrochloric acid (2.68 ml). The organic phase was separated and water extracted with dichloromethane (3×30 ml), the organic layers were washed with brine, dried and concentrated. The oily residue was chromatographed (50% petroleum ether 40-60° in dichloromethane) to afford 20c (2.98 g) as a colourless crystalline solid, mp 82.0-84.3° C. (58% yield). 1H NMR (CDCl3) δ7.49-7.43 (dd, 1H, J=9.23, 2.44 Hz); 7.29-7.11 (m, 2H); 2.57 (s, 3H); 2.39 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06391870B2 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-384ccae2082740e484f405853a213b02 |
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| Source note | uspto-grants-2002_05 |
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