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Phenethyl bromide → 4-(2-Bromoethyl)benzenesulfonyl chloride

HRID 2360593
Notes
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Reaction equation

HRID 2360593 reaction equation
[Br:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[Cl:10][S:11](O)(=[O:13])=[O:12]>C(Cl)(Cl)Cl>[Br:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([S:11]([Cl:10])(=[O:13])=[O:12])=[CH:6][CH:5]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 7666Phenethyl bromideHCID 24638Chlorosulfonic acid

Product 1

HCID 128467754-(2-Bromoethyl)benzenesulfonyl chlorideYield 80.6%

Reagents, catalysts & solvents 1

HCID 6212ChloroformSolvent2×

Procedure

To a solution of 2-bromoethylbenzene (10.0 g; 54 mmol) in 16 ml of chloroform placed at a temperature of 0° C. was added dropwise a solution of chlorosulfonic acid (162 mmol, 18.87 g; 10.82 ml) in 11 ml of chloroform. After 15 minutes at 0° C., the reaction was maintained at room temperature for 3 hours. The reaction mixture was poured onto ice, and the aqueous phase was extracted with chloroform. The combined organic phases were washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was evaporated off to give 12.34 g of crude product, which was purified by chromatography on a column of silica, eluting with chloroform (76% yield). The product obtained was used for the following reaction without further purification.

Workup

  1. customplaced at a temperature of 0° C.
  2. additionThe reaction mixture was poured onto ice
  3. extractionthe aqueous phase was extracted with chloroform
  4. washThe combined organic phases were washed with saturated sodium chloride solution
  5. dry with materialdried over anhydrous sodium sulfate
  6. customThe solvent was evaporated off

Sources & evidence

ORD record
ord-32f1c94e187f430c8540b35bf68c0823
Source dataset
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08686147B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes