Allyl bromide → HCID 18785649, compound

HRID 1107830Notes

Reaction equation

HRID 1107830 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH2:9][CH2:10][C:11]([C:13]1[NH:17][C:16]([CH3:18])=[C:15]([CH3:19])[CH:14]=1)=[O:12].Br[CH2:21][CH:22]=[CH2:23]>>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH2:9][CH2:10][C:11]([C:13]1[N:17]([CH2:23][CH:22]=[CH2:21])[C:16]([CH3:18])=[C:15]([CH3:19])[CH:14]=1)=[O:12]

Participants

3

Reactant 2

HCID 7841Allyl bromideHCID 18785654HCID 18785654, compound

Product 1

HCID 18785649HCID 18785649, compoundYield 81.7%

Procedure

The title compound was prepared as a pale yellow oil in 81.7% yield in a similar procedure to that described in Referential Example 97 by using 5-[3-(2,4-difluorophenyl)propionyl]-2,3-dimethylpyrrole and 3-bromo-1-propene.

Sources & evidence

ORD record
ord-ae9fb3fdbed94b7d8e1df51882a6b1a8
Source dataset
uspto-grants-2000_05
Patent number
US06063782

Reaction notes

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