5,6-Bis(phenylmethoxy)-1H-indole → 5,6-Dihydroxyindole

HRID 1655030ノート

反応式

HRID 1655030 の反応式
C([O:4][C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][C:13]=1[O:14]C(=O)C)[NH:10][CH:9]=[CH:8]2)(=O)C.C(OC1C=C2C(=CC=1OCC1C=CC=CC=1)NC=C2)C1C=CC=CC=1>[Fe].C(O)(=O)C>[OH:4][C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][C:13]=1[OH:14])[NH:10][CH:9]=[CH:8]2

参加物

5

反応物 2

HCID 209205,6-Bis(phenylmethoxy)-1H-indole2 回HCID 38058835,6-Diacetoxyindole

生成物 1

HCID 1146835,6-Dihydroxyindole

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 176Acetic Acid溶媒

実験手順

In a first stage, 5,6-diacetoxyindole and 5,6-dibenzyloxyindole are prepared by means of a cyclizing reduction. In the case of 5,6-dibenzyloxyindole the cyclizing reduction is carried out using iron in the presence of acetic acid. In a second stage, 5,6-dihydroxyindole is obtained:

出典と根拠

ORDレコード
ord-439111d22b684e2e8c5ea4b43c29f935
出典データセット
uspto-grants-1995_04
特許番号
US05410067

反応ノート

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