Methyl 4-(3-formylphenyl)benzoate → HCID 18626005, compound

HRID 1860012Notes

Reaction equation

HRID 1860012 reaction equation
[CH:1]([C:3]1[CH:4]=[C:5]([C:9]2[CH:14]=[CH:13][C:12]([C:15]([O:17][CH3:18])=[O:16])=[CH:11][CH:10]=2)[CH:6]=[CH:7][CH:8]=1)=[O:2].[CH:19]([O-])([O-])[O:20]C.F[C:25](F)(C(F)F)COC1C=CC(C(NCCOC2C=CC(CC(OC3C=CC(C(C)C)=CC=3)C(O)=O)=CC=2)=O)=CN=1>>[CH3:25][O:2][CH:1]([O:20][CH3:19])[C:3]1[CH:4]=[C:5]([C:9]2[CH:14]=[CH:13][C:12]([C:15]([O:17][CH3:18])=[O:16])=[CH:11][CH:10]=2)[CH:6]=[CH:7][CH:8]=1

Participants

4

Procedure

In a similar manner to that described in Example 11(a), a reaction was carried out using methyl 3′-formylbiphenyl-4-carboxylate (1.60 g), which is the product of Reference example 14(a), methyl orthoformate (3.64 ml) and amberlyst 15 (160 mg) and the reaction mixture was treated to afford the desired compound (1.91 g) as a syrup.

Workup

  1. additionthe reaction mixture was treated

Sources & evidence

ORD record
ord-5bee55ef510b4ae58da12f6df59bf424
Source dataset
uspto-grants-2003_03
Patent number
US06528525B1

Reaction notes

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