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Ethyl 2-hydroxyisobutyrate → Ethyl 2-fluoroisobutyrate

HRID 1682254
ノート
印刷プレビュー

反応式

HRID 1682254 の反応式
C1C=CN=CC=1.[FH:7].S(F)(=O)(=O)O.O[C:14]([CH3:21])([CH3:20])[C:15]([O:17][CH2:18][CH3:19])=[O:16]>>[F:7][C:14]([CH3:21])([CH3:20])[C:15]([O:17][CH2:18][CH3:19])=[O:16]
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

4

反応物 3

HCID 6653Ethyl 2-hydroxyisobutyrateHCID 24603Fluorosulfuric acidHCID 64774Pyridine, hydrofluoride (1:1)

生成物 1

HCID 10898763Ethyl 2-fluoroisobutyrate収率 52%

反応条件

温度
0 °C

実験手順

Into a 50-ml autoclave having a teflon-made internal cylinder were placed 9 ml of a hydrogen fluoride/pyridine mixture [hydrogen fluoride/pyridne =70/30 (wt/wt), containing about 300 mM of hydrogen fluoride] and 9.15 g (91.5 mM) of fluorosulfuric acid. The autoclave contents were cooled to 0° C. Thereto was added 4.0 g (30.5 mM) of ethyl 2-hydroxyisobutyrate. The resulting mixture was subjected to a reaction at 40° C. for 4 hours. After the completion of the reaction, the reaction mixture was poured into ice water. The resulting mixture was extracted with methylene chloride. The extract was dried over anhydrous sodium sulfate and subjected to vacuum distillation to remove methylene chloride. The resulting residue was subjected to distillation to obtain 2.1 g (yield: 52%) of ethyl 2-fluoroisobutyrate having a boiling point of 124°-126° C.

後処理

  1. customThe resulting mixture was subjected to a reaction at 40° C. for 4 hours
  2. customAfter the completion of the reaction
  3. extractionThe resulting mixture was extracted with methylene chloride
  4. dry with materialThe extract was dried over anhydrous sodium sulfate
  5. distillationsubjected to vacuum distillation
  6. customto remove methylene chloride
  7. distillationThe resulting residue was subjected to distillation

出典と根拠

ORDレコード
ord-6415da130c1445fe8a50521db281676d
出典データセット
uspto-grants-1992_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05175345

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート