Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzothiazole | HCID 7222 | — |
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86690036 | HCID 86690036 | — |
Reaction Steps
4-Fluorobenzoylchloride (6.5 g, 41.0 mmol) was added dropwise to a stirring solution of benzothiazole (5.4 g, 40.0 mmol) in dichloromethane (40 mL) under argon atmosphere. A catalytic amount of AlCl3 and trimethylsilylcyanide (4.1 g, 42.0 mmol) were than added into the reaction mixture. After being stirred for 15 h at room temperature, the reaction mixture was evaporated to dryness in vacuo and the residue was triturated with ether to give 3-(4-fluorobenzoyl)-2,3-dihydrobenzo[d]thiazole-2-carbonitrile, 9.3 g (82%); mp 150-151° C. 1H NMR (DMSO-d6) δ 6.71 (1H, brs, C2-H), 6.85 (1H, s, ArH), 7.04-7.07 (1H, m, ArH), 7.12-7.16 (1H, m, ArH), 7.38-7.40 (2H, m, 2×ArH), 7.52-7.54 (1H, m, ArH), 7.64-7.67 (2H, m, 2×ArH). Anal. Calcd. for (C15H9FN2OS): C, 63.37; H, 3.19; N, 9.85; S, 11.28. Found: C, 63.02; H, 3.27; N, 9.81; S, 11.31.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703951B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-45f87acaa383404d835e9c8c1ec10bfb |
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| Source note | uspto-grants-2014_04 |
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