HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538638Generated: October 31, 2026
4-Bromo-1,1,1-trifluorobutane → 2-Methyl-2-(4,4,4-trifluoro-butylsulfanyl)-propionic acid ethyl ester
https://huagongshe.com/reaction/538638
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromo-1,1,1-trifluorobutane | HCID 521006 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Ethyl 2-(acetylthio)-2-methylpropanoate | HCID 57937863 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Methyl-2-(4,4,4-trifluoro-butylsulfanyl)-propionic acid ethyl ester | HCID 59253290 | 84.3% |
Reaction Steps
To a solution of 149 g (0.785 mol) of 2-acetylsulfanyl-2-methyl-propionic acid ethyl ester in EtOH (1.2 L, degassed under nitrogen for 1 h) are added 169.7 g (0.105 mol) of sodium methoxide, followed by a solution of 150 g (0.785 mol) of 4-bromo-1,1,1-trifluoro-butane. The reaction is heated to 85° C. for 3 d. The solvent is removed under reduced pressure. The residue is dissolved in DCM (1 L) and washed with saturated aq. NaHCO3 solution (2×1 L). The organic layer is dried over Na2SO4, filtered and the filtrate is concentrated under reduced pressure to afford 171 g of 2-methyl-2-(4,4,4-trifluoro-butylsulfanyl)-propionic acid ethyl ester. Yield: 84%; ESI-MS: 259 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865744B1 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-09be35502f674df1b33e3e0e7dcb1eef |
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| Source note | uspto-grants-2014_10 |
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