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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369328Generated: October 31, 2026

Benzothiazole → HCID 86690036, compound

https://huagongshe.com/reaction/2369328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzothiazoleHCID 7222—
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductHCID 86690036HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703951B2
Source datasetuspto-grants-2014_04
ORD IDord-45f87acaa383404d835e9c8c1ec10bfb
Source noteuspto-grants-2014_04