Hydrochloric Acid → 3-Methyl-5-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-naphthalen-2-ylsulphonyl)pent-2-en-4-ynoic Acid

HRID 1278839노트

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HRID 1278839 반응식
[OH-].[Na+].[CH3:3][C:4]([C:11]#[C:12][S:13]([C:16]1[C:25]([CH3:26])=[CH:24][C:23]2[C:22]([CH3:28])([CH3:27])[CH2:21][CH2:20][C:19]([CH3:30])([CH3:29])[C:18]=2[CH:17]=1)(=[O:15])=[O:14])=[CH:5][C:6]([O:8]CC)=[O:7].C(OCC)C.O.Cl>C1COCC1>[CH3:3][C:4]([C:11]#[C:12][S:13]([C:16]1[C:25]([CH3:26])=[CH:24][C:23]2[C:22]([CH3:28])([CH3:27])[CH2:21][CH2:20][C:19]([CH3:30])([CH3:29])[C:18]=2[CH:17]=1)(=[O:15])=[O:14])=[CH:5][C:6]([OH:8])=[O:7]

참가 물질

6

실험 절차

Sodium hydroxide (400 mg, 10 mmol) is added to a solution of ethyl 3-methyl-5-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-ylsulphonyl)pent-2-en-4-ynoate (400 mg, 1.6 mmol) in 15 ml of THF. The medium is refluxed for 4 h. It is then poured into an ethyl ether/water mixture, acidified to pH 1 with concentrated hydrochloric acid solution and extracted with ethyl ether. After separation of the phases by settling, the organic phase is washed twice with water, dried over anhydrous magnesium sulphate and concentrated on a rotary evaporator under vacuum at 40° C. The residue is then triturated from heptane, after which it is filtered.

후처리

  1. temperatureThe medium is refluxed for 4 h
  2. extractionextracted with ethyl ether
  3. customAfter separation of the phases
  4. washthe organic phase is washed twice with water
  5. dry with materialdried over anhydrous magnesium sulphate
  6. concentrationconcentrated on a rotary evaporator under vacuum at 40° C
  7. customThe residue is then triturated from heptane
  8. filtrationafter which it is filtered

출처 및 근거

ORD 기록
ord-b5b0ab3ad8e745668a3f0733ed6e3545
출처 데이터셋
uspto-grants-2002_09
특허 번호
US06444709B1

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