Water → HCID 19701607、化合物

HRID 862057ノート

反応式

HRID 862057 の反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][CH2:11][O:12][CH3:13])=[C:6]([CH:9]=1)[CH2:7]O.C(N(CC)CC)C.CS([Cl:25])(=O)=O.O>ClCCl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][CH2:11][O:12][CH3:13])=[C:6]([CH:9]=1)[CH2:7][Cl:25]

参加物

6

実験手順

To a solution of 5-bromo-2-methoxymethoxybenzyl alcohol (27.2 g) and triethylamine (23 ml) in dichloromethane (550 ml) was added, at 0° C., methanesulfonyl chloride (13.9 g). The mixture was stirred for 15 hours, while warming up to room temperature. The reaction mixture was poured into water, which was subjected to extraction with ethyl acetate. The extract solution was washed with an aqueous saline solution, which was then dried (anhydrous magnesium sulfate), followed by concentration to give an oily product. The oily product was purified by means of a silica gel column chromatography (eluted with ethyl acetate/hexane) to give 5-bromo-2-methoxymethoxybenzyl chloride (21.6 g) as an oily product.

後処理

  1. extractionwas subjected to extraction with ethyl acetate
  2. washThe extract solution was washed with an aqueous saline solution, which
  3. dry with materialwas then dried (anhydrous magnesium sulfate)
  4. concentrationfollowed by concentration
  5. customto give an oily product
  6. customThe oily product was purified by means of a silica gel column chromatography (eluted with ethyl acetate/hexane)

出典と根拠

ORDレコード
ord-86398937883d410993a3db48e84943b9
出典データセット
uspto-grants-1998_02
特許番号
US05716971

反応ノート

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