Acetamidomalonic acid diethyl ester → Diethyl acetamido-(6-methoxycarbonylhex-2-ynyl)malonate
Reaction equation
[C:1]([NH:4][CH:5]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[C:6]([O:8][CH2:9][CH3:10])=[O:7])(=[O:3])[CH3:2].Br[CH2:17][C:18]#[C:19][CH2:20][CH2:21][CH2:22][C:23]([O:25][CH3:26])=[O:24]>>[C:1]([NH:4][C:5]([CH2:17][C:18]#[C:19][CH2:20][CH2:21][CH2:22][C:23]([O:25][CH3:26])=[O:24])([C:11]([O:13][CH2:14][CH3:15])=[O:12])[C:6]([O:8][CH2:9][CH3:10])=[O:7])(=[O:3])[CH3:2]Participants
3
Procedure
Under the reaction conditions described in Example 1A diethyl acetamidomalonate and methyl 7-bromohept-5-ynoate reacted to give diethyl acetamido-(6-methoxycarbonylhex-2-ynyl)malonate as a yellow oil.
Workup
- customUnder the reaction conditions
- customreacted
Sources & evidence
- ORD record
- ord-2d175f3e382745028927778f9ab194d7
- Source dataset
- uspto-grants-1981_04
- Patent number
- US04262128
Reaction notes
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