1-Methoxy-4-nitro-3-(2-nitroethenyl)-2-(phenylmethoxy)benzene → HCID 18962537, compound

HRID 1707745Notes

Reaction equation

HRID 1707745 reaction equation
[CH2:1]([O:8][C:9]1[C:19]([O:20][CH2:21]C)=[CH:18][CH:17]=[C:16]([N+:23]([O-])=O)[C:10]=1[CH:11]=[CH:12][N+]([O-])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(OC1C(OC)=CC=C([N+]([O-])=O)C=1C=C[N+]([O-])=O)C1C=CC=CC=1>>[CH2:1]([O:8][C:9]1[C:19]([O:20][CH3:21])=[CH:18][CH:17]=[C:16]2[C:10]=1[CH:11]=[CH:12][NH:23]2)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 538011151-Methoxy-4-nitro-3-(2-nitroethenyl)-2-(phenylmethoxy)benzeneHCID 539721921-Ethoxy-4-nitro-3-(2-nitroethenyl)-2-(phenylmethoxy)benzene

Product 1

HCID 18962537HCID 18962537, compound

Procedure

This compound is obtained according to the operating method described in Example lc, in which the 2-benzyloxy-3-ethoxy-6,β-dinitrostyrene is replaced with 2-benzyloxy-3-methoxy-6,β-dinitrostyrene. A white powder (yield =86%, m.p. =83°-84° C.) is obtained.

Workup

  1. customThis compound is obtained
  2. customA white powder (yield =86%, m.p. =83°-84° C.)
  3. customis obtained

Sources & evidence

ORD record
ord-c2e58fcda7624d2cbc2e2cad00bfeb96
Source dataset
uspto-grants-1994_10
Patent number
US05354870

Reaction notes

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