Dichloromethane → Benzeneethanol, 4-octyl-, 1-methanesulfonate

HRID 1505020ノート

反応式

HRID 1505020 の反応式
[CH2:1]([C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][OH:17])=[CH:11][CH:10]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].ClCCl.C(N(CC)CC)C.[CH3:28][S:29](Cl)(=[O:31])=[O:30]>O>[CH3:28][S:29]([O:17][CH2:16][CH2:15][C:12]1[CH:11]=[CH:10][C:9]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])=[CH:14][CH:13]=1)(=[O:31])=[O:30]

参加物

6

反応条件

温度
0 °C

実験手順

2-(4-Octylphenyl)ethanol (53 g) and dichloromethane (500 mL) are charged into a 1 liter three-neck round bottom flask equipped with guard tube and addition funnel. Triethylamine (83.5 g) is added, the mixture is stirred for 30 minutes, then it is cooled to 0° C. Methanesulphonyl chloride (35.2 mL) is added drop-wise at 0° C. and the mass is stirred for 3 hours at room temperature. The mass is diluted with water (700 mL) and the organic layer is separated and the aqueous layer is extracted with dichloromethane (2×250 mL). The combined organic layers is washed with saturated sodium bicarbonate (500 mL) and brine solution (500 mL). The organic layer is separated, dried with sodium sulphate, and concentrated under vacuum to obtain the title compound. Yield: 70 g.

後処理

  1. customequipped with guard tube and addition funnel
  2. stirringthe mass is stirred for 3 hours at room temperature
  3. customthe organic layer is separated
  4. extractionthe aqueous layer is extracted with dichloromethane (2×250 mL)
  5. washThe combined organic layers is washed with saturated sodium bicarbonate (500 mL) and brine solution (500 mL)
  6. customThe organic layer is separated
  7. dry with materialdried with sodium sulphate
  8. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-1a1b93bd92454003970afd1ad09040cf
出典データセット
uspto-grants-2015_12
特許番号
US09216943B2

反応ノート

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