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2-Bromo-4-chloro-1-phenylbutan-1-one → HCID 54145555, compound

HRID 460767
Notes
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Reaction equation

HRID 460767 reaction equation
[C:1]([CH:9](Br)[CH2:10][CH2:11][Cl:12])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:14][NH:15][C:16](=[S:18])[S-:17].C[NH3+]>>[CH3:14][N:15]1[C:1]([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[C:9]([CH2:10][CH2:11][Cl:12])[S:18][C:16]1=[S:17]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 202266952-Bromo-4-chloro-1-phenylbutan-1-oneHCID 7355561921160-95-2

Product 1

HCID 54145555HCID 54145555, compound

Procedure

The 3-methyl-4-phenyl-5-β-chloroethyl-4-thiazoline-2-thione is prepared in the following manner: A solution of 33 g of 1-benzoyl-1-bromo-3-chloropropane in 150 cc of absolute alcohol is added slowly to a suspension of 20 g of methyl ammonium N-methyldithiocarbamate in 150 cc of absolute alcohol. The mixture is agitated for 2 hours at ambient temperature and the solvent is then evaporated under reduced pressure. The residue is redissolved in chloroform, washed with water and the separated organic phase is dried over Na2SO4 and then evaporated to dryness.

Workup

  1. customthe solvent is then evaporated under reduced pressure
  2. dissolutionThe residue is redissolved in chloroform
  3. washwashed with water
dry with material
the separated organic phase is dried over Na2SO4
  • customevaporated to dryness
  • Sources & evidence

    ORD record
    ord-89af0c251e0f45e1ab599a0d8ab0932f
    Source dataset
    uspto-grants-1977_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04061637

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes