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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922218Generated: October 26, 2026

Methyl iodide → 2-(Methylthio)benzo[d]thiazol-6-ol

https://huagongshe.com/reaction/1922218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTriethylamineHCID 8471—
ReactantHCID 178515779HCID 178515779—
SolventDichloromethaneHCID 6344—
Product2-(Methylthio)benzo[d]thiazol-6-olHCID 4507741492%

Reaction Steps

To the ice cooled solution of 2-mercapto-benzothiazol-6-ol from step 1 (3.80 g, 20.76 mmol, 1.0 eq) in DCM (40 mL, 0.5M) at 0° C., was added triethylamine (7.29 mL, 51.91 mmol, 2.5 eq) followed by iodomethane (1.93 mL, 31.14 mmol, 1.5 eq). The reaction was stirred from 0° C. to −10° C. for 3 hours. The solvent was removed in vacuo. Water (ca. 200 mL) was added and the aqueous layer was extracted with ethyl acetate (3×150 mL). The organic layer was dried over sodium sulfate, filtered, and evaporated in vacuo to yield 2-methylsulfanyl-benzothiazol-6-ol as light green powder (3.76 g, 92%). The crude product was used in the next step without purification. M+H=198.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173689B2
Source datasetuspto-grants-2012_05
ORD IDord-86389a4ef92d4bcb9cb6114d0349d4f4
Source noteuspto-grants-2012_05