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Methane, dichloromethoxy- → 2-Formylthieno[2,3-b][1,5]benzoxazepin-4(5H)-one

HRID 1281880
Notes
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Reaction equation

HRID 1281880 reaction equation
[S:1]1[C:5]2[O:6][C:7]3[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=3[NH:9][C:10](=[O:11])[C:4]=2[CH:3]=[CH:2]1.Cl[CH:17]([O:19]C)Cl.[Cl-].[Al+3].[Cl-].[Cl-]>C(Cl)Cl>[CH:17]([C:2]1[S:1][C:5]2[O:6][C:7]3[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=3[NH:9][C:10](=[O:11])[C:4]=2[CH:3]=1)=[O:19]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 21004Methane, dichloromethoxy-HCID 6451240Aluminum(III) ChlorideHCID 18422172Thieno[2,3-b][1,5]benzoxazepin-4(5H)-one

Product 1

HCID 184221402-Formylthieno[2,3-b][1,5]benzoxazepin-4(5H)-oneYield 55.9%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

Thieno[2,3-b][1,5]benzoxazepin-4(5H)-one (1.9 g) was suspended in methylene chloride (20 ml) and dichloromethylmethyl ether (4.0 g) was added. To this reaction system was added aluminum chloride (4.6 g) under ice-cooling and the mixture was stirred for 15 minutes. The reaction mixture was poured into ice water-chloroform and the mixture was stirred at room temperature for 20 minutes. The aqueous layer was extracted 5 times with chloroform and the combined organic layer was dried over sodium sulfate. The solvent was evaporated under reduced pressure and diisopropyl ether was added to the residue. The precipitated crystals were collected by filtration to give 2-formylthieno[2,3-b][1,5]benzoxazepin-4(5H)-one (1.2 g).

Workup

  1. temperaturecooling
  2. stirringthe mixture was stirred at room temperature for 20 minutes
  3. extractionThe aqueous layer was extracted 5 times with chloroform
  4. dry with materialthe combined organic layer was dried over sodium sulfate
  5. customThe solvent was evaporated under reduced pressure and diisopropyl ether
  6. additionwas added to the residue
  7. filtrationThe precipitated crystals were collected by filtration

Sources & evidence

ORD record
ord-e750b1137c7042a394e4efff720d11be
Source dataset
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06455521B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes