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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077098Generated: October 31, 2026

Isobutyl mercaptan → N-(5-tert-butyl-isoxazol-3-yl)-2-isobutylsulfanyl-2-methyl-propionamide

https://huagongshe.com/reaction/2077098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyl mercaptanHCID 10558—
ReactantPotassium HydroxideHCID 14797—
Reactant2-bromo-N-(5-tert-butyl-isoxazol-3-yl)-2-methyl-propionamideHCID 59662626—
SolventEthanolHCID 702—
ProductN-(5-tert-butyl-isoxazol-3-yl)-2-isobutylsulfanyl-2-methyl-propionamideHCID 5970399382.5%

Reaction Steps

To a stirred solution of 82 μL (1.31 mmol) of 2-methyl-1-propanethiol in ethanol (2 mL) were added 37 mg (0.65 mmol) of KOH pellets, followed by 190 mg (0.65 mmol) 2-bromo-N-(5-tert-butyl-isoxazol-3-yl)-2-methyl-propionamide (prepared as described in step 2, method B). The reaction mixture was heated to reflux for 18 h. The reaction was cooled to room temperature. The solid (KBr) was separated by filtration and rinsed with ethanol (15 mL). The filtrate was concentrated under reduced pressure to yield 160 mg of N-(5-tert-butyl-isoxazol-3-yl)-2-isobutylsulfanyl-2-methyl-propionamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928123B2
Source datasetuspto-grants-2011_04
ORD IDord-466baef9adf345b5bf0de33f235a3db4
Source noteuspto-grants-2011_04