HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isobutyl mercaptan → N-(5-tert-butyl-isoxazol-3-yl)-2-isobutylsulfanyl-2-methyl-propionamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isobutyl mercaptan | HCID 10558 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-bromo-N-(5-tert-butyl-isoxazol-3-yl)-2-methyl-propionamide | HCID 59662626 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(5-tert-butyl-isoxazol-3-yl)-2-isobutylsulfanyl-2-methyl-propionamide | HCID 59703993 | 82.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829034B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-7fb13c4b14514bb9bb6e7d291455b61f |
| Source note | uspto-grants-2014_09 |