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Hydrochloric Acid → 7-[2,3-Dihydroxy-5-(3-hydroxyoct-1-enyl)cyclopentyl]heptanoic acid

HRID 442446
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HRID 442446 반응식
[OH:1][CH:2]1[CH:6]([O:7]C2CCCCO2)[CH2:5][CH:4]([CH:14]=[CH:15][CH:16]([OH:22])[CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])[CH:3]1[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][C:29]([OH:31])=[O:30].Cl>C(O)C>[OH:1][CH:2]1[CH:6]([OH:7])[CH2:5][CH:4]([CH:14]=[CH:15][CH:16]([OH:22])[CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])[CH:3]1[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][C:29]([OH:31])=[O:30]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 543618807-[2-Hydroxy-5-(3-hydroxyoct-1-enyl)-3-(2-tetrahydropyranyloxy)cyclopentyl]heptanoic acid

생성물 1

HCID 542209287-[2,3-Dihydroxy-5-(3-hydroxyoct-1-enyl)cyclopentyl]heptanoic acid수율 3.6%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 7-[2-hydroxy-5-(3-hydroxyoct-1-enyl)-3-(2-tetrahydropyranyloxy)cyclopentyl]heptanoic acid [0.34 g.; prepared as described above in Example 2(h)], ethanol (10 ml.), N aqueous hydrochloric acid (10 ml.) and a cation exchange resin [Dowex resin AG50W-X 8H+ (1.0 g.)] was stirred at 60°-62° C. for 8 hours. The mixture was filtered and the solid was washed with ethanol. The combined filtrate and washings were concentrated in vacuo to remove most of the ethanol, and the residue was extracted twice with diethyl ether. The combined ethereal extracts were extracted with 2N aqueous sodium carbonate solution, and the aqueous extract was acidified to pH 1 by the addition of concentrated hydrochloric acid. The resulting aqueous mixture was extracted with diethyl ether and the ethereal extract was dried over magnesium sulphate and evaporated to dryness. The residue (0.13 g.) was subjected to preparative thin-layer chromotagraphy on silica gel, using a mixture of ethyl acetate, cyclohexane and formic acid (40:40:1 by volume) as the eluent, to give 7-[2,3-dihydroxy-5-(3-hydroxyoct-1-enyl)cyclopentyl]heptanoic acid (0.01 g.), νmax 1700 cm-1, 980 cm-1.

후처리

  1. filtrationThe mixture was filtered
  2. washthe solid was washed with ethanol
  3. concentrationThe combined filtrate and washings were concentrated in vacuo
  4. customto remove most of the ethanol
  5. extractionthe residue was extracted twice with diethyl ether
  6. extractionThe combined ethereal extracts were extracted with 2N aqueous sodium carbonate solution
  7. extractionthe aqueous extract
  8. additionwas acidified to pH 1 by the addition of concentrated hydrochloric acid
  9. extractionThe resulting aqueous mixture was extracted with diethyl ether
  10. extractionthe ethereal extract
  11. dry with materialwas dried over magnesium sulphate
  12. customevaporated to dryness
  13. additiona mixture of ethyl acetate, cyclohexane and formic acid (40:40:1 by volume) as the eluent

출처 및 근거

ORD 기록
ord-c4e65718746344d1aa9fcd9e8c70351a
출처 데이터셋
uspto-grants-1977_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04045467

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