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Diethyl Malonate → Dimethyl 2-(2-isopentyl-5-methyl-2-phenylhexanoyl)malonate

HRID 2224782
Notes
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Reaction equation

HRID 2224782 reaction equation
[C:1]([O:9][CH2:10]C)(=[O:8])[CH2:2][C:3]([O:5][CH2:6]C)=[O:4].[CH2:12]([C:17]([C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)([CH2:21][CH2:22][CH:23]([CH3:25])[CH3:24])[C:18](Cl)=[O:19])[CH2:13][CH:14]([CH3:16])[CH3:15].C1(C(CCC)(CCC)C(Cl)=O)C=CC=CC=1>>[CH2:12]([C:17]([C:26]1[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=1)([CH2:21][CH2:22][CH:23]([CH3:24])[CH3:25])[C:18]([CH:2]([C:1]([O:9][CH3:10])=[O:8])[C:3]([O:5][CH3:6])=[O:4])=[O:19])[CH2:13][CH:14]([CH3:16])[CH3:15]
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 7761Diethyl MalonateHCID 116873352-Phenyl-2-propylpentanoyl chlorideHCID 865980202-isopentyl-5-methyl-2-phenylhexanoyl Chloride

Product 1

HCID 69270654Dimethyl 2-(2-isopentyl-5-methyl-2-phenylhexanoyl)malonate

Procedure

The title compound was prepared following the procedure of Example 1E, substituting dimethyl malonate for diethyl malonate, and substituting the product of Example 6D for the product of Example 1D. 1H NMR (300 MHz, CDCl3): δ 7.32 (m, 5 H), 4.54 (s, 1 H), 3.56 (s, 6 H), 2.00 (m, 4 H), 1.49 (m, 2 H), 0.87 (m, 16 H).

Sources & evidence

ORD record
ord-c3229670b61a4c24a9139e34b0595623
Source dataset
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07378414B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes