Acetic Acid → (S)-2-Hydroxymethyl-azetidine-1-carboxylic acid benzyl ester

HRID 2389514ノート

反応式

HRID 2389514 の反応式
[CH2:1]([O:8][C:9]([N:11]1[CH2:14][CH2:13][C@H:12]1[C:15](O)=[O:16])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.B.CC(O)=O.C([O-])(O)=O.[Na+]>C1COCC1.O>[CH2:1]([O:8][C:9]([N:11]1[CH2:14][CH2:13][C@H:12]1[CH2:15][OH:16])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

7

反応条件

温度
0 °C

実験手順

To a solution of (S)-Azetidine-1,2-dicarboxylic acid 1-benzyl ester (Starting material I-34f, 94 mg, 0.4 mmol) in 0.3 ml dry THF cooled to 0° C. is added dropwise 450 μl of a 1 M solution of borane in THF. The resulting solution is allowed to stir for 1 h at 0° C. and warm up to rt overnight. AcOH (1 ml) and water (1 ml) are then added as well as some saturated NaHCO3 solution in water until pH=9 and no more gas evolution occurs. The resulting aqueous phase is extracted three times with AcOEt. The combined organic phase is washed once with some saturated NaHCO3 solution in water and once with water. The solvents are evaporated in vacuo and the crude oil dried under high vacuum overnight, yielding the title compound (79 mg) in 89% as a colourless oil: tR=0.84 min (LC-3), ESI-MS (pos.): m/z 222.08 [M+H]+; 1H-NMR (CDCl3): δ (ppm) 2.00 (m, 1H, CH2CH2N), 2.22 (m, 1H, CH2CH2N), 3.78-4.01 (m, 5H, CH2N and CH2OH), 4.52 (s, 2H, OCH2Ph), 7.35 (s, 5H, Harom.). Starting material I-35e of the following Table 63 is prepared using a procedure analogous to that described for Starting material I-34e, substituting Starting material I-35f for I-34f.

後処理

  1. temperaturewarm up to rt overnight
  2. extractionThe resulting aqueous phase is extracted three times with AcOEt
  3. washThe combined organic phase is washed once with some saturated NaHCO3 solution in water and once with water
  4. customThe solvents are evaporated in vacuo
  5. customthe crude oil dried under high vacuum overnight

出典と根拠

ORDレコード
ord-775cc5e9883d4dcd80513430cf9925aa
出典データセット
uspto-grants-2012_09
特許番号
US08273740B2

反応ノート

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