3,4-Dihydroxy-5-nitrobenzaldehyde → Neopentyl 2-cyano-3-(3,4-dihydroxy-5-nitrophenyl)acrylate

HRID 1088898Notes

Reaction equation

[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([N+:11]([O-:13])=[O:12])[C:9]=1[OH:10])[CH:5]=O.[C:14]([CH2:16][C:17]([O:19][CH2:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:18])#[N:15]>>[C:14]([C:16](=[CH:5][C:4]1[CH:7]=[C:8]([N+:11]([O-:13])=[O:12])[C:9]([OH:10])=[C:2]([OH:1])[CH:3]=1)[C:17]([O:19][CH2:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:18])#[N:15]

Participants

Reactant 2

HCID 57489573,4-Dihydroxy-5-nitrobenzaldehyde

HCID 19389183Neopentyl cyanoacetate

Product 1

HCID 53667335Neopentyl 2-cyano-3-(3,4-dihydroxy-5-nitrophenyl)acrylateYield 67%

Procedure

The procedure described in Example 4 was repeated using 3,4-dihydroxy-5-nitrobenzaldehyde and neopentyl cyanoacetate. Yield 67%, m.p. 173°-179° C.

Sources & evidence

ORD record: ord-09dd03c94d684aefb94f62d8c54d29aa
Source dataset: uspto-grants-1990_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04963590

Reaction notes

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