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Ethyl p-methylbenzenesulfonate → HCID 20311111, compound

HRID 2420210
Notes
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Reaction equation

HRID 2420210 reaction equation
[CH3:1][C:2]1[O:3][C:4]2[C:10]([Cl:11])=[C:9]([CH3:12])[C:8]([Cl:13])=[CH:7][C:5]=2[N:6]=1.[CH2:14]([O:16][S:17]([C:20]1[CH:25]=[CH:24][C:23]([CH3:26])=[CH:22][CH:21]=1)(=[O:19])=[O:18])[CH3:15]>>[C:23]1([CH3:26])[CH:22]=[CH:21][C:20]([S:17]([OH:19])(=[O:16])=[O:18])=[CH:25][CH:24]=1.[CH3:1][CH:2]1[N:6]([CH2:14][CH3:15])[C:5]2[CH:7]=[C:8]([Cl:13])[C:9]([CH3:12])=[C:10]([Cl:11])[C:4]=2[O:3]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 6638Ethyl p-methylbenzenesulfonateHCID 144190195,7-Dichloro-2,6-dimethylbenzoxazole

Product 1

HCID 20311111HCID 20311111, compound

Procedure

A mixture of 2.1 g. of 2,6-dimethyl-5,7dichloro-benzoxazole and 2 g. of ethyl-p-toluene-sulfonate was heated at 150° C. for 30 minutes. By cooling, a pick cake was obtained. It was ground in a mortar by washing repeatedly with ethyl ether. The product, thus obtained, was dried and used without further purification for the synthesis of dyes.

Workup

  1. additionA mixture of 2.1 g
  2. temperatureBy cooling
  3. customa pick cake was obtained
  4. washby washing repeatedly with ethyl ether
  5. customThe product, thus obtained
  6. custom
was dried
  • customused without further purification for the synthesis of dyes
  • Sources & evidence

    ORD record
    ord-9d9400fc9b4b4a259ff7ef6a37afdcf6
    Source dataset
    uspto-grants-1978_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04110116

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes