Phosphorus oxychloride → 9-Oxo-8(12),13-trans-prostadienoic acid

HRID 1764189

反応式

HRID 1764189 の反応式
O[C@@H:2]([CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])/[CH:3]=[CH:4]/[C:5]1[CH2:6][CH2:7][C:8](=[O:19])[C:9]=1[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]([OH:18])=[O:17].C(OC=C(OC(C)=COC(C)C)C)(C)C.P(Cl)(Cl)(Cl)=O>C(Cl)Cl.CCOCC>[O:19]=[C:8]1[CH2:7][CH2:6][C:5](/[CH:4]=[CH:3]/[CH2:2][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])=[C:9]1[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]([OH:18])=[O:17]

参加物

6

反応物 3

HCID 24813Phosphorus oxychlorideHCID 5280388Pgb1HCID 88809635Isopropoxyisopropenyl ether

生成物 1

HCID 867351629-Oxo-8(12),13-trans-prostadienoic acid

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 6344Dichloromethane溶媒

実験手順

To a 250 ml roundbottom borosilicate flask containing 0.4 g of 15(S)-hydroxy-9-oxo-8(12),13-trans-prostadienoic acid in 15 ml of methylene chloride is added 5 ml of isopropoxyisopropenyl ether and 0.01 ml of phosphorus oxychloride and the flask's contents allowed to react at 20° C. for 36 hours. Next the reaction product is diluted with 25 ml of ether and washed with 50% brine and saturated brine until the solution is neutral. Next, the residue is extracted with methylene chloride, filtered, and freed of solvent under reduced pressure, dried over anhydrous magnesium sulfate, to give 15(S)-(dimethyl' isopropoxy' methyloxy)-9-oxo-8(12),13-trans-prostadienoic acid.

後処理

  1. customto react at 20° C. for 36 hours
  2. washwashed with 50% brine and saturated brine until the solution
  3. extractionNext, the residue is extracted with methylene chloride
  4. filtrationfiltered
  5. dry with materialdried over anhydrous magnesium sulfate

出典と根拠

ORDレコード
ord-4b084dce544449258417b09d4d8744d2
出典データセット
uspto-grants-1978_09
特許番号
US04115545

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