Water → (E)-Methyl 3alpha-acetoxy-5beta-chol-9(11),16,22-trien-24-oate

HRID 1671718

反応式

HRID 1671718 の反応式
[Cl-].[Cl-].C([Al+2])C.[C:6]([O:10][CH3:11])(=[O:9])[C:7]#[CH:8].[C:12]([O:15][C@@H:16]1[CH2:34][CH2:33][C@@:32]2([CH3:35])[C@H:18]([CH2:19][CH2:20][C@@H:21]3[C:31]2=[CH:30][CH2:29][C@@:28]2([CH3:36])[C@H:22]3[CH2:23][CH2:24]/[C:25]/2=[CH:26]/[CH3:27])[CH2:17]1)(=[O:14])[CH3:13].O>C(Cl)Cl>[C:12]([O:15][C@@H:16]1[CH2:34][CH2:33][C@@:32]2([CH3:35])[C@H:18]([CH2:19][CH2:20][C@@H:21]3[C:31]2=[CH:30][CH2:29][C@@:28]2([CH3:36])[C@H:22]3[CH2:23][CH:24]=[C:25]2[C@H:26]([CH3:27])/[CH:8]=[CH:7]/[C:6]([O:10][CH3:11])=[O:9])[CH2:17]1)(=[O:14])[CH3:13]

参加物

6

反応物 4

HCID 962WaterHCID 13536Methyl propiolateHCID 16686341Ethyl aluminium dichlorideHCID 25145012(3R,5R,8S,10S,13S,14S,Z)-17-Ethylidene-10,13-dimethyl-2,3,4,5,6,7,8,10,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[A]phenanthren-3-YL acetate

生成物 1

HCID 25145011(E)-Methyl 3alpha-acetoxy-5beta-chol-9(11),16,22-trien-24-oate収率 68%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
25 °C

実験手順

Ethyl aluminum dichloride (104.5 mL, 192 mmol, 1.8 M in toluene) was added to a solution of methyl propiolate (13.58 mL, 153 mmol) in DCM (100 mL) at 0° C. under inert atmosphere. The resulting solution was stirred for 15 min and then compound 1.6a (22 g, 64.3 mmol) was added. After stirring for an additional 20 min at 0° C., the temperature was raised to 25° C. and held there for a further 18 h. At this point the reaction was determined to be complete by TLC, and the mixture was poured into cold (0° C.) water (200 mL). The phases were separated and the aqueous layer was extracted with DCM (150 mL). The organic layers were combined and washed sequentially with water (200 mL) and saturated brine solution (100 mL). It was then dried over anhydrous Na2SO4 (40 g) and filtered. The filtrate was concentrated under vacuum and the resulting solid was purified by slurring in methanol (280 mL) to provide compound 1.7a (17.5 g 68%) as a white solid.

後処理

  1. stirringAfter stirring for an additional 20 min at 0° C.
  2. waitheld there for a further 18 h
  3. customThe phases were separated
  4. extractionthe aqueous layer was extracted with DCM (150 mL)
  5. washwashed sequentially with water (200 mL) and saturated brine solution (100 mL)
  6. dry with materialIt was then dried over anhydrous Na2SO4 (40 g)
  7. filtrationfiltered
  8. concentrationThe filtrate was concentrated under vacuum
  9. customthe resulting solid was purified

出典と根拠

ORDレコード
ord-53a49144e37b43e98b57ed67f34a2b7d
出典データセット
uspto-grants-2011_08
特許番号
US07994351B2

関連ノート

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