HCID 21877089, compound → HCID 21877076, compound

HRID 353091Notes

Reaction equation

HRID 353091 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:14]=[C:15]([Cl:17])[CH:16]=1)/[CH:5]=[C:6](\[C:10](=[O:13])[CH2:11][CH3:12])/[C:7](=[O:9])[CH3:8].ClC1C=C(C=C(Cl)C=1)/C=C(/C(=O)CC)\C(=O)C>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:14]=[C:15]([Cl:17])[CH:16]=1)[CH2:5][CH:6]([C:10](=[O:13])[CH2:11][CH3:12])[C:7](=[O:9])[CH3:8]

Participants

3

Reactant 2

HCID 21877089HCID 21877089, compoundHCID 60091522HCID 60091522, compound

Product 1

HCID 21877076HCID 21877076, compound

Procedure

The title compound was prepared by a similar method to that of Preparation 6 using (3Z)-3-(3,5-dichlorobenzylidene)-2,4-hexanedione and (3E)-3-(3,5-dichlorobenzylidene)-2,4-hexanedione of Preparations 18 and 19 and was obtained as yellow oil (300 mg).

Sources & evidence

ORD record
ord-ca0a44d9df814d53b892113ba1e89587
Source dataset
uspto-grants-2004_06
Patent number
US06750230B2

Reaction notes

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