Lithium Hydroxide → Equol

HRID 2171750ノート

反応式

HRID 2171750 の反応式
O[CH2:2][C@H:3]([C:13]1[CH:18]=[CH:17][C:16]([OH:19])=[CH:15][CH:14]=1)[CH2:4][C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][C:6]=1[OH:12].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[OH-].[Li+]>C1COCC1>[CH:18]1[C:13]([C@H:3]2[CH2:2][O:12][C:6]3[CH:7]=[C:8]([OH:11])[CH:9]=[CH:10][C:5]=3[CH2:4]2)=[CH:14][CH:15]=[C:16]([OH:19])[CH:17]=1

参加物

5

反応物 3

HCID 3939Lithium HydroxideHCID 11776TriphenylphosphineHCID 71744429(S)-4-(3-hydroxy-2-(4-hydroxyphenyl)propyl)benzene-1,3-diol

生成物 1

HCID 91469Equol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a mixture of alcohol of formula (9) (50 g) and triphenyl phosphine (151 g) in THF (2.5 L) diisopropyl azodicarboxylate (116.5 g) in THF (500 mL) was added at 15-20° C. and maintained at that temperature for 1-2 hours. About 5% lithium hydroxide solution (1000 mL) was added into the reaction mass and extracted with MTBE (3×750 mL) to remove the organic impurities. The pH of the aqueous layer was adjusted to 1-4 by dilute hydrochloric acid (250 mL). The reaction mass was maintained at RT for 5-6 hours and the product was filtered off. The crude product was taken with IPA (7.5 vol) and added water (22.5 vol). The reaction mass was then maintained at RT for 12-14 hours. The solid was filtered and dried at 50-55° C. for 10-12 hours to afford the title compound.

後処理

  1. additionwas added at 15-20° C.
  2. temperaturemaintained at that temperature for 1-2 hours
  3. extractionextracted with MTBE (3×750 mL)
  4. customto remove the organic impurities
  5. filtrationthe product was filtered off
  6. additionadded water (22.5 vol)
  7. temperatureThe reaction mass was then maintained at RT for 12-14 hours
  8. filtrationThe solid was filtered
  9. customdried at 50-55° C. for 10-12 hours

出典と根拠

ORDレコード
ord-9fecbd60cacf4fa2aa96634c9e67e3ab
出典データセット
uspto-grants-2015_06
特許番号
US09051291B2

反応ノート

読み込み中…