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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Triethylamine → Ethyl 2,2-difluoropent-4-enoate

HRID 231654
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HRID 231654 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 145971243-[(Trifluoroethenyl)oxy]prop-1-ene2회HCID 14597125HCID 14597125, 화합물

생성물 1

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

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-4abcc008e00841fbb135759453ba7e96
출처 데이터셋
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04847401

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