1-Bromooctane → HCID 22618805, compound
Reaction equation
C([O:4][CH2:5][C:6]([NH:17]C(=O)C)([CH3:16])[CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([OH:15])[CH:10]=1)(=O)C.[CH2:21](Br)[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28].[ClH:30].NC(CCC1C=CC=CC=1OCCCCCCC)(CCC)CO>>[ClH:30].[NH2:17][C:6]([CH3:16])([CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([O:15][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[CH:10]=1)[CH2:5][OH:4]Participants
4
Procedure
2-Acetamido-4-(3-hydroxyphenyl)-2-methylbutyl acetate and octyl bromide were used in the same manner as working example 52 (9) and (10) to give the subject compound as white crystals, melting at 130-132° C.
Sources & evidence
- ORD record
- ord-5e1208c0fb2e4d10967aa1daa5958d92
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06372800B1
Reaction notes
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