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Dimethyl Sulfide → HCID 20977333、化合物

HRID 882498
ノート
印刷プレビュー

反応式

HRID 882498 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].CSC>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

4

反応物 2

HCID 1068Dimethyl SulfideHCID 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 127 (25.0 g, 153 mmol) in THF (400 mL), cooled to 0° C., was added BH3.DMS (49.5 mL, 460 mmol), following which the cooling bath was removed. The resulting mixture was gradually warmed to reflux and maintained overnight. This was then cooled in an ice-bath and quenched by the slow addition of large excess of MeOH. After stirring at RT for about 2 h, the excess solvent was removed under reduced pressure. The residue was again treated with MeOH and evaporated. The process was repeated thrice. 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 (128) 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. additionwas added BH3
  2. customwas removed
  3. temperatureThe resulting mixture was gradually warmed
  4. temperatureto reflux
  5. temperaturemaintained overnight
  6. temperatureThis was then cooled in an ice-bath
  7. customquenched by the slow addition of large excess of MeOH
  8. customthe excess solvent was removed under reduced pressure
  9. additionThe residue was again treated with MeOH
  10. customevaporated
  11. washeluted (0 to 15% (9:1 MeOH—NH3)-DCM gradient)

出典と根拠

ORDレコード
ord-4f599f7f1754496aac2d7bc5c39b0348
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08993807B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート