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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73234Generated: October 27, 2026

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

https://huagongshe.com/reaction/73234

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 numberUS08829034B2
Source datasetuspto-grants-2014_09
ORD IDord-7fb13c4b14514bb9bb6e7d291455b61f
Source noteuspto-grants-2014_09