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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639776Generated: November 1, 2026

tert-Butyl mercaptan → Methyl 3-[(tert-butylthio)diazenyl]-6-fluoro-2-methylbenzoate

https://huagongshe.com/reaction/1639776

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl mercaptanHCID 6387—
ReactantPotassium AcetateHCID 517044—
ReactantSodium NitriteHCID 23668193—
ReactantBenzoic acid, 3-amino-6-fluoro-2-methyl-, methyl esterHCID 59334575—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductMethyl 3-[(tert-butylthio)diazenyl]-6-fluoro-2-methylbenzoateHCID 5933453199.3%

Reaction Steps

To a solution of methyl 3-amino-6-fluoro-2-methylbenzoate (12.0 g, 65.5 mmol) in hydrochloric acid (6 N, 200 mL) was added a solution of sodium nitrite (4.97 g, 72.1 mmol) in water (10 mL) at 0° C., and the mixture was stirred for 2 hr. An aqueous potassium acetate solution (30%) was added to the reaction solution at 0° C. to adjust the reaction solution to pH 4, and a solution of 2-methylpropane-2-thiol (8.12 mL, 72.1 mmol) in ethanol (10 mL) was added. The reaction solution was stirred at room temperature for 12 hr, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure to give the title compound (18.5 g, yield 99%) as a crudely purified product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110585B2
Source datasetuspto-grants-2012_02
ORD IDord-1cbf438207524dc98b6243840b6d4f17
Source noteuspto-grants-2012_02