Sodium Hydroxide → Tert-butoxy(4-iodo-2-methyl-5,6,7,8-tetrahydro[1]benzothieno[2,3-b]pyridin-3-yl)acetic acid

HRID 63938ノート

反応式

HRID 63938 の反応式
[C:1]([O:5][CH:6]([C:11]1[C:12]([I:25])=[C:13]2[C:20]3[CH2:21][CH2:22][CH2:23][CH2:24][C:19]=3[S:18][C:14]2=[N:15][C:16]=1[CH3:17])[C:7]([O:9]C)=[O:8])([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+]>O1CCCC1>[C:1]([O:5][CH:6]([C:11]1[C:12]([I:25])=[C:13]2[C:20]3[CH2:21][CH2:22][CH2:23][CH2:24][C:19]=3[S:18][C:14]2=[N:15][C:16]=1[CH3:17])[C:7]([OH:9])=[O:8])([CH3:4])([CH3:2])[CH3:3]

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 66603844HCID 66603844、化合物

生成物 1

HCID 67606758Tert-butoxy(4-iodo-2-methyl-5,6,7,8-tetrahydro[1]benzothieno[2,3-b]pyridin-3-yl)acetic acid収率 88%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
60 °C

実験手順

To a solution of Methyl tert-butoxy(4-iodo-2-methyl-5,6,7,8-tetrahydro[1]benzothieno[2,3-b]pyridin-3-yl)acetate (Preparation 10, 63.95 g, 135 mmol) in tetrahydrofuran (1 L) and methylated spirit (1 L) was dropwise added aqueous sodium hydroxide (1 M, 811 mL, 811 mmol). The resulting mixture was stirred at 60° C. for 90 minutes and then allowed to cool to room temperature overnight. The volatile solvents were removed in vacuo, and the remaining aqueous residue was diluted with water (400 mL) and extracted with tert-butyl methyl ether (600 mL). The organic layer was washed with water (400 mL) and then cooled on ice. 2 M hydrochloric acid was added to pH 5 and the resulting solids were collected by filtration, washing with water. The solid was dissolved in 2-methyl tetrahydrofuran (300 mL) and stirred for 10 minutes. An aqueous layer had appeared and this was separated. The aqueous layer was extracted with 2-methyl tetrahydrofuran (2×300 mL). The combined organic layers were dried over MgSO4 and concentrated in vacuo to give the title compound as a pale yellow solid, 54.35 g, in an 88% yield. 1H NMR (400 MHz, CDCl3) δ ppm 1.27 (s, 9 H), 1.81-1.93 (m, 4 H), 2.65 (s, 3 H), 2.76-2.88 (m, 2 H), 3.20-3.27 (m, 2 H), 6.13 (s, 1 H), 9.66 (br s, 1 H).

後処理

  1. temperatureto cool to room temperature overnight
  2. customThe volatile solvents were removed in vacuo
  3. additionthe remaining aqueous residue was diluted with water (400 mL)
  4. extractionextracted with tert-butyl methyl ether (600 mL)
  5. washThe organic layer was washed with water (400 mL)
  6. temperaturecooled on ice
  7. addition2 M hydrochloric acid was added to pH 5
  8. filtrationthe resulting solids were collected by filtration
  9. washwashing with water
  10. dissolutionThe solid was dissolved in 2-methyl tetrahydrofuran (300 mL)
  11. stirringstirred for 10 minutes
  12. customthis was separated
  13. extractionThe aqueous layer was extracted with 2-methyl tetrahydrofuran (2×300 mL)
  14. dry with materialThe combined organic layers were dried over MgSO4
  15. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-ff85187fcc6f499dac3b5d41478b8fdb
出典データセット
uspto-grants-2016_09
特許番号
US09447116B2

反応ノート

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