Diazomethane → HCID 20310681, compound

HRID 259031Notes

Reaction equation

HRID 259031 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=2

Participants

4

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

  1. 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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