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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Benzene → 1,3-Cyclohexadiene-1-carboxylic acid, 2,6,6-trimethyl-, ethyl ester

HRID 436719
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HRID 436719 반응식
[CH3:1][C:2]1[CH:3]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[C:4]([CH3:9])([CH3:8])[CH:5]=[CH:6][CH:7]=1.C1(C)C=CC(S(O)(=O)=O)=CC=1.C1C=CC=CC=1>CCCCC>[CH3:1][C:2]1[CH:7]=[CH:6][CH2:5][C:4]([CH3:8])([CH3:9])[C:3]=1[C:10]([O:12][CH2:13][CH3:14])=[O:11]
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참가 물질

5

반응물 3

HCID 241BenzeneHCID 6101p-Toluenesulfonic acidHCID 118199Ethyl alpha-safranate

생성물 1

HCID 1182011,3-Cyclohexadiene-1-carboxylic acid, 2,6,6-trimethyl-, ethyl ester

시약·촉매·용매 1

HCID 8003Pentane용매

실험 절차

A mixture of 2.0 g of 2,6,6-trimethyl-1-ethoxycarbonyl-2,4-cylohexadiene [prepared according to the process indicated in Example 1], 100 mg of p-toluenesulphonic acid and 25 ml of anhydrous benzene were refluxed for 4 hours in a nitrogen atmosphere. The resulting solution was diluted with pentane, washed with a 5 % solution of sodium bicarbonate, then with water, and then dried over Na2SO4 and concentrated.

후처리

  1. customprepared
  2. temperaturewere refluxed for 4 hours in a nitrogen atmosphere
  3. washwashed with a 5 % solution of sodium bicarbonate
  4. dry with materialwith water, and then dried over Na2SO4
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-062c75b6511c45838ce5dacbd2b6898a
출처 데이터셋
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04028278

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