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Benzene → HCID 12906807, compound

HRID 2052549
Notes
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Reaction equation

HRID 2052549 reaction equation
[CH3:1][C:2]1([CH3:7])[NH:6][CH2:5][CH2:4][S:3]1.C1C=CC=CC=1.[Br:14][CH:15]([Br:19])[C:16](Cl)=[O:17].C(N(CC)CC)C>O>[CH3:1][C:2]1([CH3:7])[N:6]([C:16](=[O:17])[CH:15]([Br:19])[Br:14])[CH2:5][CH2:4][S:3]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 241BenzeneHCID 8471TriethylamineHCID 79184Dibromoacetyl chlorideHCID 880152,2-Dimethylthiazolidine

Product 1

HCID 12906807HCID 12906807, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

To a mixture of 3.5 g. of 2,2-dimethyl thiazolidine, 50 ml. of benzene and 7.1 g. of dibromoacetyl chloride mixed in an ice bath was added 3.1 g. of triethylamine dropwise with stirring and continued cooling. When reaction was complete, the mixture was poured into water and the benzene layer separated, dried over magnesium sulfate and the benzene removed under vacuum. Yield was 8.5 g. of a dark oil.

Workup

  1. additionTo a mixture of 3.5 g
  2. additionwas added 3.1 g
  3. temperaturecontinued cooling
  4. customWhen reaction
  5. customthe benzene layer separated
  6. dry with materialdried over magnesium sulfate
  7. customthe benzene removed under vacuum

Sources & evidence

ORD record
ord-3d995a5236204a62b9a91e84bd389014
Source dataset
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04186130

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes