3,5-Diphenyl4-[(2-methoxyethoxy)methoxy]-phenyl decyl ether → 2,6-Diphenyl-4-decyloxy-phenol

HRID 1281437ノート

反応式

HRID 1281437 の反応式
[CH2:1]([O:11][C:12]1[CH:17]=[C:16]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:15]([O:24]COCCOC)=[C:14]([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[CH:13]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]>C(Cl)Cl.[Zn+2].[Br-].[Br-]>[C:31]1([C:14]2[CH:13]=[C:12]([O:11][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10])[CH:17]=[C:16]([C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=3)[C:15]=2[OH:24])[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=1

参加物

4

反応物 1

HCID 222374833,5-Diphenyl4-[(2-methoxyethoxy)methoxy]-phenyl decyl ether

生成物 1

HCID 222375862,6-Diphenyl-4-decyloxy-phenol収率 79.1%

試薬・触媒・溶媒 2

HCID 10421208Zinc bromide触媒HCID 6344Dichloromethane溶媒

実験手順

A mixture of 3,5-diphenyl-4-[(2-methoxyethoxy)methoxy]-phenyl decyl ether (0.880 g, 1.793 mmol) and ZnBr2 (2.019 g, 8.967 mmol) in methylene chloride (10 ml) under nitrogen was stirred at room temperature. After ˜48 h, the reaction mixture was concentrated in vac and the residue was taken up in EtOAc (60 ml) and saturated NaHCO3 solution (20 ml). The layers were shaken and separated and the organic layer was washed with saturated NaHCO3 solution (2×10 ml), water (3×10 ml), brine (1×10 ml), dried over Na2SO4, filtered and the filtrate concentrated in vac and dried. The residue was purified by flash chromatography (hexane and 1% EtOAc/Hex) to give the product as a light brown oil (0.571 g, 79%); 1H NMR (400 MHz, DMSO-d6) δ 0.83-0.88 (m, 3H), 1.20-1.36 (m, 12H), 1.36-1.45 (m, 2H), 1.65-1.73 (m, 2H), 3.96 (t, J=6.6 Hz, 2H), 6.77 (s, 2H), 7.31-7.36 (m, 2H), 7.40-7.45 (m, 4H), 7.54-7.58 (m, 4H), 7.80 (s, 1H); IR (film) 3550, 2940, 1600, 1460, 1180 cm−1; mass spectrum [EI], m/z 402 M+.

後処理

  1. concentrationthe reaction mixture was concentrated in vac
  2. stirringThe layers were shaken
  3. customseparated
  4. washthe organic layer was washed with saturated NaHCO3 solution (2×10 ml), water (3×10 ml), brine (1×10 ml)
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationthe filtrate concentrated in vac
  8. customdried
  9. customThe residue was purified by flash chromatography (hexane and 1% EtOAc/Hex)

出典と根拠

ORDレコード
ord-e106c9297f93465b87eb7a8d856771e7
出典データセット
uspto-grants-2002_09
特許番号
US06451827B2

反応ノート

読み込み中…