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Methanol → HCID 54520137, compound

HRID 1579109
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Reaction equation

HRID 1579109 reaction equation
[CH:1]1([C:7]2[CH:8]=[CH:9][C:10]3[CH:13]=[C:12]([C:14]([OH:16])=[O:15])[C:11]=3[CH:17]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.O.[CH3:19]O>S(=O)(=O)(O)O>[CH3:19][O:15][C:14]([C:12]1[C:11]2[CH:17]=[C:7]([CH:1]3[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]3)[CH:8]=[CH:9][C:10]=2[CH:13]=1)=[O:16]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 887MethanolHCID 962WaterHCID 21484415HCID 21484415, compound

Product 1

HCID 54520137HCID 54520137, compound

Reagents, catalysts & solvents 1

HCID 1118Sulfuric AcidSolvent

Procedure

A solution of 15 g of 5-cyclohexyl-1-benzocyclobutenecarboxylic acid in 150 ml of absolute methanol and 1.5 ml of concentrated sulphuric acid is boiled for 14 hours under reflux whilst excluding water. The reaction mixture is evaporated in vacuo at 30°C to a volume of approx. 30 ml and the evaporation residue is partitioned between three times 200 ml of ether and twice 200 ml of ice water. The combined organic phases are successively washed with saturated sodium bicarbonate solution and water, dried over sodium sulphate and evaporated in vacuo. Distillation of the evaporation residue in a high vacuum yields 5-cyclohexyl-1-benzocyclobutenecarboxylic acid methyl ester in the fraction boiling at approx. 150°C/0.07 mm Hg.

Workup

  1. temperatureunder reflux
  2. customThe reaction mixture is evaporated in vacuo at 30°C to a volume of approx. 30 ml
  3. customthe evaporation residue is partitioned between three times 200 ml of ether and twice 200 ml of ice water
  4. washThe combined organic phases are successively washed with saturated sodium bicarbonate solution and water
  5. dry with materialdried over sodium sulphate
  6. customevaporated in vacuo
  7. distillationDistillation of the evaporation residue in a high vacuum

Sources & evidence

ORD record
ord-4496f2d8eda14b498b577a9da4f67c7a
Source dataset
uspto-grants-1976_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US03940434

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes