Benzyl Bromide → HCID 22127020、化合物

反応式

[OH:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[C:4]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH:3]=1.[CH2:17](Br)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[CH2:17]([O:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[C:4]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH:3]=1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1

参加物

反応物 2

HCID 7498Benzyl Bromide

HCID 13080945Ethyl 4-hydroxynaphthalene-2-carboxylate

生成物 1

HCID 22127020HCID 22127020、化合物

実験手順

By alkylating ethyl 4-hydroxy-naphthalene-2-carboxylate [J. Agric. Chem Soc. Japan 24, 313 (1950)] with benzyl bromide in an analogous manner to that described in Example 14(a) there was obtained ethyl 4-benzyloxy-naphthalene-2-carboxylate as an almost colourless solid; MS: 21 6 (M)+.

出典と根拠

ORDレコード: ord-65f91c3e6f03448d89cfaf15cd77963d
出典データセット: uspto-grants-2000_04
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US06051712

反応ノート

読み込み中…