Triphenylphosphine → HCID 19387449, compound

HRID 1757306Notes

Reaction equation

HRID 1757306 reaction equation
[C:1]1([P:7]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:20][C:21]([CH2:23][CH2:24][CH2:25][Cl:26])=[O:22]>>[Cl-:26].[CH3:20][C:21]([CH2:23][CH2:24][CH2:25][P+:7]([C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)=[O:22]

Participants

3

Reactant 2

HCID 11776TriphenylphosphineHCID 799932-Pentanone, 5-chloro-

Product 1

HCID 19387449HCID 19387449, compoundYield 82%

Procedure

The title compound was prepared from triphenylphosphine and 3-chloropropyl methyl ketone as described in Example 1 in a yield of 82%.

Sources & evidence

ORD record
ord-5dbbc17aaf2242838056385994e6ddc5
Source dataset
uspto-grants-1995_08
Patent number
US05445724

Reaction notes

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