Benzyl Alcohol → 2-Benzyl-D-arabinose

HRID 251525

反応式

HRID 251525 の反応式
[O:1]=[CH:2][C@H:3]([C@@H:5]([C@@H:7]([CH2:9][OH:10])[OH:8])[OH:6])[OH:4].[CH2:11](O)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(Cl)(=O)C>CC(OC)(C)C>[CH2:11]([C@@:3]([C@@H:5]([C@@H:7]([CH2:9][OH:10])[OH:8])[OH:6])([OH:4])[CH:2]=[O:1])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1

参加物

5

反応条件

温度
35 °C

実験手順

D-Arabinose (50 kg, 330.04 moles) and benzyl alcohol (132.2 kg, 4.33 equivalents) were stirred and heated to 35° C. Acetyl chloride (10.9 kg, 0.42 equivalents), keeping the temperature<45° C., then stirred 50° C. overnight. The mixture was cooled to 20° C. and diluted with MTBE (600 kg). The mixture was stirred for 0.5-5 h. The solids were collected by filtration and washed with MTBE (2×40 kg). The material was dried in a filter drier. 2-Benzyl-D-arabinose was obtained as an off-white solid, 70.9 kg (88.6%). 1H NMR (300 MHz, DMSO-d6): δ 7.32 (m, 5H), 4.76 (s, 1H), 4.66 (d, J=12 Hz, 1H), 4.59 (m, 3H), 4.45 (d, J=12 Hz, 1H), 3.70 (m, 4H), 3.47 (dd, J=12, 3 Hz, 1H).

後処理

  1. customthe temperature<45° C.
  2. temperatureThe mixture was cooled to 20° C.
  3. stirringThe mixture was stirred for 0.5-5 h
  4. filtrationThe solids were collected by filtration
  5. washwashed with MTBE (2×40 kg)
  6. customThe material was dried in
  7. filtrationa filter drier

出典と根拠

ORDレコード
ord-301a52a638024057b592d80ee4ee0143
出典データセット
uspto-grants-2011_01
特許番号
US07863453B2

関連ノート

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