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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288714Generated: October 26, 2026

Isopropyl iodide → Methyl 3-amino-2-methyl-6-(1-methylethylsulphenyl)-benzoate

https://huagongshe.com/reaction/1288714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantSodium SulfideHCID 14804—
ReactantMethyl 3-amino-2-methyl-6-thiocyanatobenzoateHCID 14801188—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductMethyl 3-amino-2-methyl-6-(1-methylethylsulphenyl)-benzoateHCID 5417721975.3%

Reaction Conditions

Temperature5 °C

Reaction Steps

A suspension of methyl 3-amino-2-methyl-6-thiocyanatobenzoate (22.2 g) in ethanol was added to a solution of sodium sulphide (26.6 g) in water. The resultant mixture was stirred at room temperature for 1 hour and then cooled to 5° C. 2-Iodopropane (19.36 g) was added and the mixture was allowed to warm to room temperature and stirred for 2 hours. It was evaporated to dryness and the residue was suspended in aqueous sodium chloride solution and extracted with dichloromethane. The organic layer was dried (MgSO4) and filtered. The filtrate was evaporated to dryness to give methyl 3-amino-2-methyl-6-(1-methylethylsulphenyl)benzoate (18 g) as a yellow oil NMR(CDCl3) 1.2(d,6H) 2.0(s,3H) 3.0(m,1H) 3.8(bs,2H) 3.9(s,1H) 6.5(d,1H) 7.0(d,1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05747424
Source datasetuspto-grants-1998_05
ORD IDord-2facbc2a476e4873862188ab8c3c6792
Source noteuspto-grants-1998_05