Diisopropylamine → 4-Tert-butyl 1-methyl 2-(4-chlorophenyl)succinate

HRID 158462Notes

Reaction equation

HRID 158462 reaction equation
[Br:33][CH2:34][C:35](=[O:36])[O:37][C:38]([CH3:39])([CH3:40])[CH3:41].[CH2:42]1[O:43][CH2:44][CH2:45][CH2:46]1.[CH3:1][CH2:2][CH2:3][CH2:4][Li:5].[CH3:26][CH:27]([N-:28][CH:29]([CH3:30])[CH3:31])[CH3:32].[CH:6]([NH:7][CH:8]([CH3:9])[CH3:10])([CH3:11])[CH3:12].[Cl:13][c:14]1[cH:15][cH:16][c:17]([CH2:20][C:21](=[O:22])[O:23][CH3:24])[cH:18][cH:19]1.[Li+:25]>>[Cl:13][c:14]1[cH:15][cH:16][c:17]([CH:20]([C:21](=[O:22])[O:23][CH3:24])[CH2:34][C:35](=[O:36])[O:37][C:38]([CH3:39])([CH3:40])[CH3:41])[cH:18][cH:19]1

Participants

8

Reactant 7

HCID 7912DiisopropylamineHCID 8028TetrahydrofuranHCID 28486Lithium ionHCID 79177tert-Butyl bromoacetateHCID 104196Methyl 4-chlorophenylacetateHCID 5062348DiisopropylamideHCID 178418339Butyllithium

Product 1

HCID 666183864-Tert-butyl 1-methyl 2-(4-chlorophenyl)succinate

Sources & evidence

ORD record
ord-8454513485454697bb241f4ecbc51ed8
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction notes

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