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Triethylamine → Ethyl 2,2-difluoropent-4-enoate

HRID 231654
ノート
印刷プレビュー

反応式

HRID 231654 の反応式
[CH2:1]([O:4]C(F)=C(F)F)[CH:2]=C.C(N(CC)CC)C.[F:17][C:18]([F:25])([CH2:22][CH:23]=[CH2:24])[C:19](F)=[O:20]>C(O)C>[F:17][C:18]([F:25])([CH2:22][CH:23]=[CH2:24])[C:19]([O:4][CH2:1][CH3:2])=[O:20]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8471TriethylamineHCID 145971243-[(Trifluoroethenyl)oxy]prop-1-ene2 回HCID 14597125HCID 14597125、化合物

生成物 1

HCID 14049931Ethyl 2,2-difluoropent-4-enoate

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

実験手順

The start of the reaction in the reactor is indicated by a rise in temperature within the reaction chamber 5 from originally -74° C. to about -45° C. During the rest of the reaction period the temperature in the reaction chamber varies from about -45° C. to about -55° C. The reaction mixture from outlet conduit 18 containing the 1,2,2-trifluorovinyl allyl ether is conducted to a stirred solution of 434 g (600 mL, 4.3 mol) of triethylamine in 358 g (450 mL, 7.8 mol) of absolute ethanol cooled in an ice bath. Upon warming to the ice bath temperature, the 1,2,2-trifluorovinyl allyl ether spontaneously rearranges to 2,2-difluoro-4-pentenoyl fluoride, which in the presence of ethanol reacts to yield the desired ethyl 2,2-difluoro-4-pentenoate. The reaction mixture is divided into two equal batches which are treated separately. The following describes the workup of one batch.

後処理

  1. customThe start of the reaction in the reactor
  2. customis indicated by a rise in temperature within the reaction chamber 5 from originally -74° C. to about -45° C
  3. customDuring the rest of the reaction period the temperature in the reaction chamber varies from about -45° C. to about -55° C
  4. temperaturecooled in an ice bath
  5. customreacts

出典と根拠

ORDレコード
ord-4abcc008e00841fbb135759453ba7e96
出典データセット
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04847401

反応ノート

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