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Dimethyl Sulfide → L-(-)-Tryptophanol

HRID 885901
ノート
印刷プレビュー

反応式

HRID 885901 の反応式
[NH2:1][C@H:2]([C:13](O)=[O:14])[CH2:3][C:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[NH:6][CH:5]=1.S(C)C>C1COCC1>[NH2:1][C@@H:2]([CH2:3][C:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[NH:6][CH:5]=1)[CH2:13][OH:14]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 1068Dimethyl SulfideHCID 6305L-Tryptophan

生成物 1

HCID 6951149L-(-)-Tryptophanol収率 92%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
70 °C

実験手順

To a stirred solution of (S)-tryptophan (4.0 g, 20.0 mmol) in THF (100 mL) at 0° C. was slowly added BH3.Me2S complex (5.9 mL, 10M solution in THF, 59.0 mmol). The reaction mixture was heated to 70° C. for 16 h and, after cooling, the excess borane was quenched by the addition of MeOH (10 mL) at 0° C. The reaction mixture was then concentrated in vacuo and the resultant white solid was dissolved in EtOAc (100 mL) and washed with aqueous 20% NaOH solution (2×70 mL). The organic layer was then extracted into aqueous 2M HCl (2×100 mL). The combined acidic aqueous layers were basified to pH 14 (addition of solid NaOH) and were re-extracted with EtOAc (2×150 mL). The combined organic fractions were washed with brine (70 mL), dried over MgSO4, filtered and concentrated in vacuo to give the title compound (3.5 g, 92%) as a white solid that required no further purification. δH (CD3OD) 7.46 (1H, d, J 7.9 Hz), 7.21 (1H, d, J 8.0 Hz), 6.96 (3H, m), 3.79 (1H, dd, J 11.3 and 3.6 Hz), 3.54 (1H, dd, J 11.2 and 6.2 Hz), 3.05 (1H, m), 2.80 (1H, m), 2.61 (1H, m). Exchangeable protons were not observed.

後処理

  1. temperatureafter cooling
  2. customthe excess borane was quenched by the addition of MeOH (10 mL) at 0° C
  3. concentrationThe reaction mixture was then concentrated in vacuo
  4. dissolutionthe resultant white solid was dissolved in EtOAc (100 mL)
  5. washwashed with aqueous 20% NaOH solution (2×70 mL)
  6. extractionThe organic layer was then extracted into aqueous 2M HCl (2×100 mL)
  7. additionThe combined acidic aqueous layers were basified to pH 14 (addition of solid NaOH)
  8. extractionwere re-extracted with EtOAc (2×150 mL)
  9. washThe combined organic fractions were washed with brine (70 mL)
  10. dry with materialdried over MgSO4
  11. filtrationfiltered
  12. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-2f98ec1e7c594ff388378fc983600664
出典データセット
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08242116B2

反応ノート

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