Hydrochloric Acid → 2,20-Dichloro-6,7,9,10,12,13,15,16-octahydro-22H-dibenzo[n,q][1,4,7,10,13]-pentaoxacyclo-octadecin

HRID 2049105

반응식

HRID 2049105 반응식
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[CH2:9][C:10]1[CH:15]=[C:14]([Cl:16])[CH:13]=[CH:12][C:11]=1[OH:17].Cl[CH2:19][CH2:20][O:21][CH2:22][CH2:23][O:24][CH2:25][CH2:26][O:27][CH2:28][CH2:29]Cl.[OH-].[Na+].Cl>CCCCO>[Cl:16][C:14]1[CH:13]=[CH:12][C:11]2[O:17][CH2:29][CH2:28][O:27][CH2:26][CH2:25][O:24][CH2:23][CH2:22][O:21][CH2:20][CH2:19][O:1][C:2]3[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=3[CH2:9][C:10]=2[CH:15]=1

참가 물질

6

실험 절차

10 g (0.037 mole) bis(2-hydroxy-5-chlorophenyl)-methane and 8.6 g (0.037 mole) 1,11-dichloro-3,6,9-trioxaundecane are dissolved in 100 ml n-BuOH. To this is added 6.5 g 50% aqueous sodium hydroxide. The resulting solution is heated to reflux for 15 hours, acidified with ethereal HCl, and solvent stripped in vacuo. The resulting gum is chromatographed on Neutral Alumina IV, eluting with ether/ethyl acetate. Appropriate fractions are collected, combined and recrystallized from methanol to yield 3.65 g white crystalline solid; m.p. 143.5°-144°. Yield: 23%.

후처리

  1. temperatureThe resulting solution is heated
  2. temperatureto reflux for 15 hours
  3. customThe resulting gum is chromatographed on Neutral Alumina IV
  4. washeluting with ether/ethyl acetate
  5. customAppropriate fractions are collected
  6. customrecrystallized from methanol

출처 및 근거

ORD 기록
ord-fcb16beadb9d4d88b428fe0f5ef73338
출처 데이터셋
uspto-grants-1980_04
특허 번호
US04196250

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