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

HRID 1263026
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HRID 1263026 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-1ca3ee7b9f7241898525a0d88e408b54
출처 데이터셋
uspto-grants-1984_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04454343

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