2',4'-Dihydroxyacetophenone → HCID 13881975, compound
Reaction equation
Br[CH:2]([CH3:12])[CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9]CC)=[O:8].[CH3:13][C:14]([C:16]1[CH:17]=[CH:18][C:19]([OH:23])=[CH:20][C:21]=1[OH:22])=[O:15]>>[C:14]([C:16]1[CH:17]=[CH:18][C:19]([O:23][CH:2]([CH3:12])[CH2:3][CH2:4][CH2:5][CH2:6][C:7]([OH:9])=[O:8])=[CH:20][C:21]=1[OH:22])(=[O:15])[CH3:13]Participants
3
Procedure
Following the procedure of Example 40, 4.74 g. of ethyl 6-bromoheptanoate and 3.04 g. of 2,4-dihydroxyacetophenone were reacted in the usual manner and the resulting product hydrolyzed to give the title product, m.p. about 116°-118° C.
Sources & evidence
- ORD record
- ord-67193bb0aacd4a14b2fd689deac91c59
- Source dataset
- uspto-grants-1987_04
- Patent number
- US04661505
Reaction notes
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