Hydrochloric Acid → 2,3,5,6-Tetrafluoro-4-[(1-methylethoxy)methyl]-benzyl alcohol

HRID 1085719

反応式

HRID 1085719 の反応式
[Na].[CH:2]([OH:5])([CH3:4])[CH3:3].Br[CH2:7][C:8]1[C:15]([F:16])=[C:14]([F:17])[C:11]([CH2:12][OH:13])=[C:10]([F:18])[C:9]=1[F:19].Cl>O>[F:17][C:14]1[C:15]([F:16])=[C:8]([CH2:7][O:5][CH:2]([CH3:4])[CH3:3])[C:9]([F:19])=[C:10]([F:18])[C:11]=1[CH2:12][OH:13]

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 3776IsopropanolHCID 5360545SodiumHCID 11265752(4-(Bromomethyl)-2,3,5,6-tetrafluorophenyl)methanol

生成物 1

HCID 147188942,3,5,6-Tetrafluoro-4-[(1-methylethoxy)methyl]-benzyl alcohol

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
40 °C

実験手順

Sodium (1.0 g) was added to dry isopropanol (200 cm3), maintained at 40° C. under an atmosphere of dry nitrogen. After dissolution was complete, 4-(bromomethyl)-2,3,5,6-tetrafluorobenzyl alcohol (10.9 g) was added and the reaction was stirred for 16 hours, at the ambient temperature. The reaction mixture was poured into water, acidified with dilute aqueous hydrochloric acid, and extracted into ethyl acetate. The combined organic extracts were washed with water, dried over anhydrous magnesium sulphate, and concentrated by evaporation of the solvent under reduced pressure. The residue was combined with the product of a similar reaction and distilled under reduced pressure to give 2,3,5,6-tetrafluoro-4-[(1-methyl-ethoxy)methyl]-benzyl alcohol (0.8 g).

後処理

  1. dissolutionAfter dissolution
  2. extractionextracted into ethyl acetate
  3. washThe combined organic extracts were washed with water
  4. dry with materialdried over anhydrous magnesium sulphate
  5. concentrationconcentrated by evaporation of the solvent under reduced pressure
  6. customThe residue was combined with the product of a similar reaction
  7. distillationdistilled under reduced pressure

出典と根拠

ORDレコード
ord-2cd9a152c81b408792f7f38e7c8616bb
出典データセット
uspto-grants-1991_04
特許番号
US05010200

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