Triethylamine → (2S)-2-[(1S)-5-methoxy-2,3-dihydro-1H-inden-1-yl]butanoic Acid

HRID 2235846ノート

反応式

HRID 2235846 の反応式
[CH3:1][O:2][C:3]1[CH:11]=[C:10]2[C:6]([C:7]([C@H:12]([CH2:16][CH3:17])[C:13]([OH:15])=[O:14])=[CH:8][CH2:9]2)=[CH:5][CH:4]=1.CCN(CC)CC>CCO.C1COCC1>[CH3:1][O:2][C:3]1[CH:11]=[C:10]2[C:6](=[CH:5][CH:4]=1)[C@H:7]([C@H:12]([CH2:16][CH3:17])[C:13]([OH:15])=[O:14])[CH2:8][CH2:9]2

参加物

5

反応物 2

HCID 8471TriethylamineHCID 11364955HCID 11364955、化合物

生成物 1

HCID 11345339(2S)-2-[(1S)-5-methoxy-2,3-dihydro-1H-inden-1-yl]butanoic Acid収率 95%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of the product obtained in Example 20 (105 g, 453 mmol), ClRh(PPh3)3 (21.0 g, 22.7 mmol), and Et3N (68.8 g, 679.5 mmol) in EtOH (945 mL) and THF (105 mL) was shaken in a 2-L pressure bottle under H2 (60 psi) for 16 h. The solvents were removed under reduced pressure and the residue was taken up in a mixture of HCl (1.5 L, 1 N aqueous solution) and CH2Cl2 (1.5 L) and stirred. The aqueous layer was extracted with CH2Cl2 (2×250 mL). The combined organic layers were washed with HCl (1 L, 1 N aqueous solution) and stirred with NaOH (1 L, 1 N aqueous solution). The organic layer was extracted with NaOH (2×0.5 L, 1 N aqueous solution). The combined aqueous layer was washed with CH2Cl2 (2×250 mL), and acidified (pH 2.0-3.0) by a slow addition of HCl (37% aqueous solution) while maintaining the temperature below 15° C. The acidic mixture was extracted with CH2Cl2 (2×1.5 L). The combined organic phases were washed with water (2×0.5 L) until a pH of 5.0-6.0 was reached, and brine, dried over Na2SO4, filtered, and then concentrated under reduced pressure. The product (101.0 g, 95% yield, 96.8% ee) was obtained as a light yellow oil.

後処理

  1. customThe solvents were removed under reduced pressure
  2. additionthe residue was taken up in a mixture of HCl (1.5 L, 1 N aqueous solution) and CH2Cl2 (1.5 L)
  3. extractionThe aqueous layer was extracted with CH2Cl2 (2×250 mL)
  4. washThe combined organic layers were washed with HCl (1 L, 1 N aqueous solution)
  5. stirringstirred with NaOH (1 L, 1 N aqueous solution)
  6. extractionThe organic layer was extracted with NaOH (2×0.5 L, 1 N aqueous solution)
  7. washThe combined aqueous layer was washed with CH2Cl2 (2×250 mL)
  8. additionby a slow addition of HCl (37% aqueous solution)
  9. temperaturewhile maintaining the temperature below 15° C
  10. extractionThe acidic mixture was extracted with CH2Cl2 (2×1.5 L)
  11. washThe combined organic phases were washed with water (2×0.5 L) until a pH of 5.0-6.0
  12. dry with materialbrine, dried over Na2SO4
  13. filtrationfiltered
  14. concentrationconcentrated under reduced pressure
  15. customThe product (101.0 g, 95% yield, 96.8% ee) was obtained as a light yellow oil

出典と根拠

ORDレコード
ord-f7e820f17f4d4a2eb336be6bbfd65036
出典データセット
uspto-grants-2010_05
特許番号
US07714004B2

反応ノート

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