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Trifluoroacetic acid → HCID 18319554, 화합물

HRID 1699387
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HRID 1699387 반응식
I[C:2]1[C:12]2[O:11][CH2:10][CH2:9][C:8]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=[CH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.[F:18][C:19]([F:24])([F:23])C(O)=O.[Na]>CN1CCCC1=O.[Cu]I>[F:18][C:19]([F:24])([F:23])[C:2]1[C:12]2[O:11][CH2:10][CH2:9][C:8]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=[CH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1
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참가 물질

6

반응물 3

HCID 6422Trifluoroacetic acidHCID 5360545SodiumHCID 18319552HCID 18319552, 화합물

생성물 1

HCID 18319554HCID 18319554, 화합물

시약·촉매·용매 2

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매HCID 13387N-methyl-2-pyrrolidone용매

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온도
160 °C

실험 절차

A mixture of ethyl 2,3-dihydro-9-iodo-1-benzoxepin-4-carboxylate (1.00 g), trifluoroacetic acid, sodium salt (1.58 g), and copper(I) iodide (1.11 g) in 1-methyl-2-pyrrolidinone (10 ml) was stirred at 160° C. under nitrogen atmosphere for 6 hours and partitioned between ethyl acetate and 1N hydrochloric acid. The aqueous layer was extracted twice with ethyl acetate. The combined organic layer was washed successively with saturated aqueous sodium bicarbonate and brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The residue was purified by column chromatography on silica gel using a mixture of n-hexane and ethyl acetate (4:1) to give ethyl 2,3-dihydro-9-trifluoromethyl-1-benzoxepin-4-carboxylate (0.93 g).

후처리

  1. custompartitioned between ethyl acetate and 1N hydrochloric acid
  2. extractionThe aqueous layer was extracted twice with ethyl acetate
  3. washThe combined organic layer was washed successively with saturated aqueous sodium bicarbonate and brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customevaporated in vacuo
  6. customThe residue was purified by column chromatography on silica gel using
  7. additiona mixture of n-hexane and ethyl acetate (4:1)

출처 및 근거

ORD 기록
ord-966bf1ceaada4bbba6743429b9100494
출처 데이터셋
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06346527B1

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