Diazomethane → HCID 20310681, compound
Reaction equation
[O:1]=[C:2]1[C:8]2[CH:9]=[CH:10][C:11]([C:13]([OH:15])=[O:14])=[CH:12][C:7]=2[CH:6]=[CH:5][C:4]2[CH:16]=[CH:17][CH:18]=[CH:19][C:3]1=2.[N+](=[CH2:22])=[N-]>O1CCOCC1>[O:1]=[C:2]1[C:8]2[CH:9]=[CH:10][C:11]([C:13]([O:15][CH3:22])=[O:14])=[CH:12][C:7]=2[CH:6]=[CH:5][C:4]2[CH:16]=[CH:17][CH:18]=[CH:19][C:3]1=2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
5.0 G. of 5-oxo-5H-dibenzo[a,d]cycloheptene-2-carboxylic acid (as prepared above) is suspended in 50 ml. of dioxane, added to excess ethereal diazomethane, and stirred until dissolution is complete. The solution is then evaporated to dryness to yield methyl (5-oxo-5H-dibenzo[a,d]cyclohepten-2-yl)carboxylate (m.p. 115°-116° C).
Workup
- customThe solution is then evaporated to dryness
Sources & evidence
- ORD record
- ord-6a0807457bb3489abd94a6d0ab21cd10
- Source dataset
- uspto-grants-1977_07
- Patent number
- US04035509
Reaction notes
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