Hydrochloric Acid → 1,3-Dihydro-1-hydroxy-2,1-benzoxaborol-5-ol

HRID 1020784

反応式

HRID 1020784 の反応式
[OH:1][C:2]1[CH:3]=[CH:4][C:5]([B:10]2[O:14][C:13](C)(C)C(C)(C)[O:11]2)=[C:6]([CH:9]=1)C=O.[BH4-].[Na+].O.Cl>CO>[B:10]1([OH:11])[C:5]2[CH:4]=[CH:3][C:2]([OH:1])=[CH:9][C:6]=2[CH2:13][O:14]1

参加物

6

反応条件

温度
0 °C

実験手順

Into a 100-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen was placed a solution of 5-hydroxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde (5.5 g, 22 mmol, 1.0 equiv) in methanol (25 mL). This was followed by the addition of NaBH4 (1.24 g, 32.6 mmol, 1.5 equiv) in several batches at 0° C. The resulting solution was stirred for 10 min at 0° C., then it was concentrated under vacuum to get rid of half methanol at low temperature. To the residual solution was added water (6 mL) and HCl (6M, 14.5 mL) dropwise at 0° C. The resulting solution was stirred overnight at room temperature. Then it was concentrated under vacuum at low temperature to remove MeOH. The solid was collected by filtration. This resulted in 2.0 g of benzo[c][1,2]oxaborole-1,5(3H)-diol as a white solid.

後処理

  1. customInto a 100-mL 3-necked round-bottom flask purged
  2. temperaturemaintained with an inert atmosphere of nitrogen
  3. concentrationit was concentrated under vacuum
  4. customto get rid of half methanol at low temperature
  5. stirringThe resulting solution was stirred overnight at room temperature
  6. concentrationThen it was concentrated under vacuum at low temperature
  7. customto remove MeOH
  8. filtrationThe solid was collected by filtration
  9. customThis resulted in 2.0 g of benzo[c][1,2]oxaborole-1,5(3H)-diol as a white solid

出典と根拠

ORDレコード
ord-56a1b6da687c4867a7bb0d3aa7aa6186
出典データセット
uspto-grants-2014_05
特許番号
US08716478B2

関連ノート

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