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HCID 58027707、化合物 → HCID 20977333、化合物

HRID 1189982
ノート
印刷プレビュー

反応式

HRID 1189982 の反応式
[OH:1][CH:2]([C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([OH:12])[CH:7]=1)[CH2:3][C:4]#[N:5]>C1COCC1>[NH2:5][CH2:4][CH2:3][CH:2]([C:6]1[CH:7]=[C:8]([OH:12])[CH:9]=[CH:10][CH:11]=1)[OH:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 58027707HCID 58027707、化合物

生成物 1

HCID 20977333HCID 20977333、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a stirred solution of the nitrile 21.16 (25.0 g, 153 mmol) in THF, cooled to 0° C., was added BH3-DMS (49.5 mL, 460 mmol), following which the cooling bath was removed. The resulting mixture was boiled under reflux overnight, cooled in an ice-bath and quenched by the slow addition of large excess of MeOH. After stirring at room temperature for 2 h, the excess solvent was removed under reduced pressure. The residue was again treated with MeOH and evaporated. The process was repeated three times. The brown oil was then applied onto a flash silica gel column and eluted (0 to 15% (9:1 MeOH—NH3)-DCM gradient) to give 3-(3-amino-1-hydroxypropyl)phenol (21.17) as a brown solid. Yield (25.0 g, 97%); 1H NMR (400 MHz, DMSO-d6) δ 7.04-7.09 (m, 1H), 6.74 (s, 1H), 6.70 (d, J=7.6 Hz, 1H), 6.58 (dd, J=8.0, 2.0 Hz, 1H), 4.55 (dd, J=7.2, 5.6 Hz, 1H), 2.57-2.66 (m, 2H), 1.56-1.62 (m, 2H).

後処理

  1. customwas removed
  2. temperatureunder reflux overnight
  3. temperaturecooled in an ice-bath
  4. customquenched by the slow addition of large excess of MeOH
  5. customthe excess solvent was removed under reduced pressure
  6. additionThe residue was again treated with MeOH
  7. customevaporated
  8. washeluted (0 to 15% (9:1 MeOH—NH3)-DCM gradient)

出典と根拠

ORDレコード
ord-70bd427623654fbeb954b2fbb5284202
出典データセット
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08674137B2

反応ノート

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