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Methanol → HCID 178419086、化合物

HRID 747359
ノート
印刷プレビュー

反応式

HRID 747359 の反応式
[OH:1][C:2]1[N:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4](O)=[O:5].B.C1COCC1.CO>C1COCC1>[OH:5][CH2:4][C:3]1[C:2]([OH:1])=[N:10][CH:9]=[CH:8][CH:7]=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

5

反応物 3

HCID 887MethanolHCID 2723981Borane;tetrahydrofuranHCID 178418543HCID 178418543、化合物

生成物 1

HCID 178419086HCID 178419086、化合物収率 29%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
80 °C

実験手順

To a suspension of 2-Hydroxynicotinic acid (1.01 g, 7.26 mmol) in THF (2 mL) was added BH3.THF (1.0 m in THF, 18 mL, 18 mmol) and the mixture was heated to 80° C. for 18 hours. MeOH (2 mL) was added and the mixture was heated to 80° C. for an additional 2 hours before being cooled to room temperature and concentrated under reduced pressure. The resultant crude syrup was repeatedly dissolved in MeOH (5 mL) and concentrated (3×). Purification by column chromatography on silica gel (20:1—CH2Cl2:MeOH) afforded the desired alcohol (260 mg, 29%) as a white solid. 1H NMR (CD3OD) δ 4.50 (s, 2H), 6.43 (t, 1H, J=6.6 Hz), 7.34 (d, 1H, J=4.5 Hz), 7.65 (d, 1H, J=6.3 Hz).

後処理

  1. temperaturethe mixture was heated to 80° C. for an additional 2 hours
  2. temperaturebefore being cooled to room temperature
  3. concentrationconcentrated under reduced pressure
  4. dissolutionThe resultant crude syrup was repeatedly dissolved in MeOH (5 mL)
  5. concentrationconcentrated (3×)
  6. customPurification by column chromatography on silica gel (20:1—CH2Cl2:MeOH)

出典と根拠

ORDレコード
ord-89d938e29a12449fb5640ff2bf0912aa
出典データセット
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07396840B2

反応ノート

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