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Methanol → Methyl 6-Bromohexanoate

HRID 565146
ノート
印刷プレビュー

反応式

HRID 565146 の反応式
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O-:9])=[O:8].[CH3:10]O>>[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9][CH3:10])=[O:8]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 887MethanolHCID 69998686-Bromohexanoate

生成物 1

HCID 4170292Methyl 6-Bromohexanoate収率 93%

反応条件

温度
25 °C

実験手順

To a 2 liter round bottom flask, charge with 99.7 g (0.511 mol) of 6-bromohexanoate (Aldrich Chemi(al Co., Milwaukee, Wis.) and 1 liter of methanol, was bubbled hydrogen chloride gas for 1-2 minutes. The mixture was stirred at 20-30° C. for 18 h and then concentrated via rotary evaporation. The residue was diluted with 500 mL of diethyl ether and washed with 150 mL of de-ionized water, 200 mL of saturated sodium bicarbonate, and then once again with 200 mL of de-ionized water. The organic phase was dried over anhydrous magnesium sulfate, filtered and concentrated via rotary evaporation. The residue was distiled under vacuum to afford 99.6 g of the product (1) as a colorless oil (93%): b.P.=93-96° C. at 3 mm Hg: 1H NMR (d6-DMSO) d 3.57 (3H, s), 3.51 (2H, t), 2.30 (2H, t), 1.78 (2H, pentet) and 1.62-1.28 (4H, mr) ppm.

後処理

  1. customwas bubbled hydrogen chloride gas for 1-2 minutes
  2. concentrationconcentrated via rotary evaporation
  3. additionThe residue was diluted with 500 mL of diethyl ether
  4. washwashed with 150 mL of de-ionized water, 200 mL of saturated sodium bicarbonate
  5. dry with materialThe organic phase was dried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated via rotary evaporation
  8. customThe residue was distiled under vacuum

出典と根拠

ORDレコード
ord-de8789db3dd0441484f1882b9d3d744c
出典データセット
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06171577B2

反応ノート

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