Acetic Acid → 2-(1-Trityl-1H-tetrazol-5-YL)phenylboronic acid

HRID 250815

反応式

HRID 250815 の反応式
[C:1]1([C:7]2[N:11]([C:12]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[N:10]=[N:9][N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[B:31](OC(C)C)([O:36]C(C)C)[O:32]C(C)C.C(O)(=O)C>C1COCC1>[C:12]([N:11]1[C:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=2[B:31]([OH:36])[OH:32])=[N:8][N:9]=[N:10]1)([C:25]1[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1)([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1

参加物

5

反応物 3

HCID 176Acetic AcidHCID 21531Triisopropyl borateHCID 104303585-phenyl-1-trityl-1H-tetrazole

生成物 1

HCID 103427452-(1-Trityl-1H-tetrazol-5-YL)phenylboronic acid収率 69.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-25 °C

実験手順

A solution of 5-phenyl-1-trityl-1H-tetrazole (70.0 g, 180.20 mmol, 1.00 equiv) in THF (dried) (560 mL) was placed in a flask that had been purged and maintained with an inert atmosphere of nitrogen. The mixture was cooled to −25° C. Butyllithium was added to quench the trace of water in the reaction mixture until the color of the mixture remained red for at least 5 minutes. Butyllithium (80.0 mL, 2.5 mol/L) was then added dropwise to the mixture over a period of about 40 minutes at a temperature below −25° C. The temperature of the mixture was raised to −5° C., and the mixture was stirred at −5° C. for 3 hours. The mixture was then cooled to −25° C. and triisopropyl borate (50.8 g, 270.11 mmol, 1.50 equiv) was added dropwise. The mixture was warmed to temperature in the range of 25-35° C. and stirred for 2 hours. The mixture was cooled again in the range of 0-5° C., and 3% aqueous acetic acid (470 mL) was slowly added over 30-40 minutes. The mixture was stirred for 30-40 minutes and then filtered. The crude product was washed with water (2×300 mL) and dried over reduced pressure. The crude product was then purified by re-crystallization from EtOAc (1 g/15 ml) to yield 54 g (69%) of the title compound as a white solid. ES m/z: [M+H]+ calcd for C26H21BN4O2 433.1, found 433.1.

後処理

  1. customthat had been purged
  2. temperaturemaintained with an inert atmosphere of nitrogen
  3. additionButyllithium was added
  4. customto quench the trace of water in the reaction mixture until the color of the mixture
  5. waitremained red for at least 5 minutes
  6. additionButyllithium (80.0 mL, 2.5 mol/L) was then added dropwise to the mixture over a period of about 40 minutes at a temperature below −25° C
  7. temperatureThe temperature of the mixture was raised to −5° C.
  8. temperatureThe mixture was then cooled to −25° C.
  9. temperatureThe mixture was warmed to temperature in the range of 25-35° C.
  10. stirringstirred for 2 hours
  11. additionwas slowly added over 30-40 minutes
  12. stirringThe mixture was stirred for 30-40 minutes
  13. filtrationfiltered
  14. washThe crude product was washed with water (2×300 mL)
  15. customdried over reduced pressure
  16. customThe crude product was then purified by re-crystallization from EtOAc (1 g/15 ml)

出典と根拠

ORDレコード
ord-c906216ea51f478abd6430f1d8acb79a
出典データセット
uspto-grants-2011_01
特許番号
US07863309B2

関連ノート

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