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Hydrochloric Acid → 6-Isopropoxy-1,3-dihydro-1-hydroxy-2,1-benzoxaborole

HRID 529198
ノート
印刷プレビュー

反応式

HRID 529198 の反応式
[OH:1][C:2]1[CH:11]=[CH:10][C:5]2[CH2:6][O:7][B:8]([OH:9])[C:4]=2[CH:3]=1.[H-].[Na+].Br[CH:15]([CH3:17])[CH3:16].Cl>CN(C=O)C>[CH:15]([O:1][C:2]1[CH:11]=[CH:10][C:5]2[CH2:6][O:7][B:8]([OH:9])[C:4]=2[CH:3]=1)([CH3:17])[CH3:16]
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

6

反応物 4

HCID 313Hydrochloric AcidHCID 63582-BromopropaneHCID 24758Sodium hydrideHCID 529192911,3-Dihydro-2,1-benzoxaborole-1,6-diol

生成物 1

HCID 513512686-Isopropoxy-1,3-dihydro-1-hydroxy-2,1-benzoxaborole収率 61.5%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒

反応条件

温度
0 °C

実験手順

H181 (150 mg, 1.0 mmol) was dissolved in DMF (8.0 mL) and cooled to 0° C. with ice bath. To this solution under nitrogen were added in sequence NaH (60% in mineral oil, 160 mg, 4.0 mmol) and 2-bromopropane (0.40 mL, 4.0 mmol). The reaction mixture was stirred for 2 d then treated with 1.0 M HCl (10.0 mL). After extraction with ethyl acetate, the organic phase was washed with water and brine, and dried over anhydrous Na2SO4. The residue after rotary evaporation was purified by column chromatography over silica gel to give the title compound (118 mg, 61.5% yield). 1H NMR (300 MHz, DMSO-d6): δ 9.10 (s, 1H), 7.27 (d, J=8.4 Hz, 1H), 7.23 (d, J=2.4 Hz, 1H), 7.01 (dd, J=8.1 & 2.4 Hz, 1H), 4.90 (s, 2H), 4.63-4.53 (m, 1H) and 1.27 (d, J=6 Hz, 6H) ppm; Mp: 62-65° C.

後処理

  1. extractionAfter extraction with ethyl acetate
  2. washthe organic phase was washed with water and brine
  3. dry with materialdried over anhydrous Na2SO4
  4. customThe residue after rotary evaporation
  5. customwas purified by column chromatography over silica gel

出典と根拠

ORDレコード
ord-af778ed661cf476ab9750f215fe2b0cb
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09346834B2

反応ノート

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