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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369325Generated: November 1, 2026

Acetyl chloride → HCID 60165810, compound

https://huagongshe.com/reaction/2369325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantBenzothiazoleHCID 7222—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductHCID 60165810HCID 60165810—

Reaction Steps

Acetylchloride (4.00 g, 51.0 mmol) was added dropwise to a stirring solution of benzothiazole (6.75 g, 50.0 mmol) in dichloromethane (40 mL) under argon atmosphere. A catalytic amount of AlCl3 and trimethylsilylcyanide (5.1 g, 52.0 mmol) were than added into the reaction mixture. After being stirred for 17 h at room temperature, the reaction mixture was evaporated to dryness in vacuo and the residue was triturated with ether to give 3-acetyl-2,3-dihydrobenzo[d]thiazole-2-carbonitrile, 8.2 g (80%); mp 92-93° C. 1H NMR (DMSO-d6) δ 2.39 (3H, s, Me), 7.05 (1H, s, ArH), 7.16-7.26 (2H, m, 2×ArH), 7.49-7.51 (1H, m, ArH), 7.65 (1H, brs, C2-H). Anal. Calcd. for (C10H8N2OS): C, 58.80; H, 3.95; N, 13.72; S, 15.70. Found: C, 58.85; H, 3.95; N, 13.78; S, 15.76.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703951B2
Source datasetuspto-grants-2014_04
ORD IDord-52f3767442b8441aac175a1315635801
Source noteuspto-grants-2014_04