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Peracetic Acid → HCID 71281752、化合物

HRID 1481784
ノート
印刷プレビュー

反応式

HRID 1481784 の反応式
[CH2:1]([O:8][C:9]1[N:24]=[CH:23][C:22](I)=[C:21]([O:26][CH2:27][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[C:10]=1[C:11]([O:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([Mg]Cl)(C)C.[Li+].[Cl-].B(OC(C)C)(OC(C)C)[O:42]C(C)C.C(OO)(=O)C>C1COCC1.O>[CH2:1]([O:8][C:9]1[N:24]=[CH:23][C:22]([OH:42])=[C:21]([O:26][CH2:27][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[C:10]=1[C:11]([O:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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

7

反応物 4

HCID 6585Peracetic AcidHCID 21531Triisopropyl borateHCID 71281816HCID 71281816、化合物HCID 178461733HCID 178461733、化合物

生成物 1

HCID 71281752HCID 71281752、化合物収率 36.5%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
-45 °C

実験手順

Into a solution of benzyl 2,4-bis(benzyloxy)-5-iodonicotinate (1.0 g, 1.8 mmol) in THF (8.0 mL) at −45° C. was added a solution of i-PrMgCl—LiCl (1.3 M×2.8 mL, 3.6 mmol) dropwise. The mixture was stirred at −45° C. for 30 min, into which triisopropyl borate (0.87 mL, 3.78 mmol) was added dropwise. After stirring at −45° C. for 15 min, the temperature was allowed to rise to room temperature slowly. The mixture was stirred at room temperature for 1.5 h then cooled to −20° C., into which peracetic acid (32%, 0.79 mL, 3.78 mmol) was added. The mixture was stirred at room temperature for another 30 min before it was treated with water (50 mL). The mixture was extracted with ethyl acetate. The organic layers were combined and washed with brine, dried over sodium sulfate, evaporated and purified by silica chromatography (0-30% ethyl acetate in hexanes) to give benzyl 2,4-bis(benzyloxy)-5-hydroxynicotinate (0.29 g, 36%).

後処理

  1. additionwas added dropwise
  2. customto rise to room temperature
  3. stirringThe mixture was stirred at room temperature for 1.5 h
  4. additionwas added
  5. stirringThe mixture was stirred at room temperature for another 30 min before it
  6. extractionThe mixture was extracted with ethyl acetate
  7. washwashed with brine
  8. dry with materialdried over sodium sulfate
  9. customevaporated
  10. custompurified by silica chromatography (0-30% ethyl acetate in hexanes)

出典と根拠

ORDレコード
ord-32f3dc230177495eada0c348f9c4138f
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09409905B2

反応ノート

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