Ammonia → Allyl 4-allyloxy-3-aminobenzoate

HRID 1736358ノート

反応式

HRID 1736358 の反応式
[CH2:1]([O:4][C:5]1[CH:16]=[CH:15][C:8]([C:9]([O:11][CH2:12][CH:13]=[CH2:14])=[O:10])=[CH:7][C:6]=1[N+:17]([O-])=O)[CH:2]=[CH2:3].C(OC1C=C([N+]([O-])=O)C=CC=1C(OCC=C)=O)C=C.N>CO>[CH2:1]([O:4][C:5]1[CH:16]=[CH:15][C:8]([C:9]([O:11][CH2:12][CH:13]=[CH2:14])=[O:10])=[CH:7][C:6]=1[NH2:17])[CH:2]=[CH2:3]

参加物

5

実験手順

The above nitro compound was reduced by the method described in example 1, for the reduction of allyl 2-allyloxy-4-nitrobenzoate, except that the solvent was methanol, and using an aqueous solution of ammonia in place of sodium bicarbonate in the work-up, to give allyl 4-allyloxy-3-aminobenzoate.

出典と根拠

ORDレコード
ord-4b065fbabcf24293b417dcacb350f0a1
出典データセット
uspto-grants-1996_07
特許番号
US05541178

反応ノート

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