3,4-dihydro-2H-pyran → 2-[(3-Bromophenyl)methoxy]oxane

HRID 326905

反応式

HRID 326905 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH2:8][OH:9])[CH:5]=[CH:6][CH:7]=1.[O:10]1[CH:15]=[CH:14][CH2:13][CH2:12][CH2:11]1.Br.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]([CH2:8][O:9][CH:11]2[CH2:12][CH2:13][CH2:14][CH2:15][O:10]2)[CH:5]=[CH:6][CH:7]=1

参加物

5

反応物 3

HCID 80803,4-dihydro-2H-pyranHCID 80811Triphenylphosphonium bromideHCID 851413-Bromobenzyl alcohol

生成物 1

HCID 152820642-[(3-Bromophenyl)methoxy]oxane

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

The alcohol of Step 1 (41.23 mmol), dihydropyran (12.5 mL, 137 mmol) and triphenylphosphine hydrobromide (725 mg, 2.11 mmol) were mixed together in 200 mL of CH2Cl2 and stirred for 2 days. The solvent was then evaporated and the title product was purified by flash chromatography on silica using EtOAc:toluene.

後処理

  1. customThe solvent was then evaporated
  2. customthe title product was purified by flash chromatography on silica

出典と根拠

ORDレコード
ord-c2ae1008ecfd42148dc93d7121468a10
出典データセット
uspto-grants-1993_12
特許番号
US05270324

関連ノート

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