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Sodium ethoxide → Ethyl 6,6,6-trichloro-3,3-dimethyl-4-hexenoate

HRID 359172
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HRID 359172 반응식
Br[CH:2]([CH2:12][C:13]([Cl:16])([Cl:15])[Cl:14])[C:3]([CH3:11])([CH3:10])[CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6].[O-]CC.[Na+]>O1CCCC1>[Cl:14][C:13]([Cl:15])([Cl:16])[CH:12]=[CH:2][C:3]([CH3:10])([CH3:11])[CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6]
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참가 물질

4

반응물 2

HCID 2723922Sodium ethoxideHCID 12607835Ethyl 4-bromo-6,6,6-trichloro-3,3-dimethylhexanoate

생성물 1

HCID 53438823Ethyl 6,6,6-trichloro-3,3-dimethyl-4-hexenoate수율 82%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

Two milliliters of a solution of anhydrous tetrahydrofuran containing 709 mg (2 mmoles) of ethyl 4-bromo-6,6,6-trichloro-3,3-dimethylhexanoate was added dropwise to a suspension of 163 mg (2.4 mmoles) of sodium ethoxide in 20 ml of anhydrous tetrahydrofuran. The mixture was stirred at room temperature for about 16 hours, poured into ice water and extracted with diethyl ether. The extract was dried over magnesium sulfate and then distilled to give 448 mg (82% yield) of ethyl 6,6,6-trichloro-3,3-dimethyl-4-hexenoate, b.p. 83°-85°/0.1 mm.

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후처리

  1. extractionextracted with diethyl ether
  2. dry with materialThe extract was dried over magnesium sulfate
  3. distillationdistilled

출처 및 근거

ORD 기록
ord-f122b52601e04442817bb2d69414c808
출처 데이터셋
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04999451

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