HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Bromine → 1-Bromo-3-methyl-3-trifluoromethylthio-butan-2-one

HRID 1249145
Notes
Print preview

Reaction equation

HRID 1249145 reaction equation
[CH3:1][C:2]([S:7][C:8]([F:11])([F:10])[F:9])([CH3:6])[C:3](=[O:5])[CH3:4].[Br:12]Br>C(Cl)(Cl)Cl>[Br:12][CH2:4][C:3](=[O:5])[C:2]([CH3:1])([S:7][C:8]([F:10])([F:11])[F:9])[CH3:6]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24408BromineHCID 131173002-Methyl-2-(trifluoromethylthio)butan-3-one

Product 1

HCID 131173011-Bromo-3-methyl-3-trifluoromethylthio-butan-2-oneYield 85%

Reagents, catalysts & solvents 1

HCID 6212ChloroformSolvent

Conditions

Temperature
40 °C

Procedure

3-Methyl-3-trifluoromethylthio-butan-2-one was dissolved in chloroform and bromine was added dropwise at 20° C. at such a rate that decolorization occurred continuously. Addition was stopped when the color persisted, the reaction mixture was further stirred at 40° C. 1-Bromo-3-methyl-3-trifluoromethylthio-butan-2-one of boiling point 56° C./0.4 mbar was obtained in a yield of 85%. ##STR13##

Workup

  1. additionAddition

Sources & evidence

ORD record
ord-081686470629422b9e3c3b323def5179
Source dataset
uspto-grants-1986_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04629732

Reaction notes

Loading…

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes