反応 #674319

ord-6796e4ab1c0444cba33a0d3bcfbade61

反応方程式

CC(C)(C)OC(=O)N1CCC[C@@H]1CO
compound
CC(C)(C)OC(=O)N1CCC[C@@H]1CO
tert-butyl (R)-2-(hydroxymethyl)pyrrolidine-1-carboxylate
Oc1ccccc1
phenol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CC(C)OC(=O)N=NC(=O)OC(C)C
diisopropyl azodicarboxylate
CC(C)(C)OC(=O)N1CCC[C@@H]1COc1ccccc1
tert-butyl (R)-2-(phenoxymethyl)pyrrolidine-1-carboxylate

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出the solution was extracted with aqueous 3N NaOH
  2. 2
    洗浄The organic layer was washed with brine
  3. 3
    乾燥dried over MgSO4
  4. 4
    濃縮concentrated in vacuo

実験手順

To an ice-cold solution of the compound from Step 1 (2.60 g, 12.9 mmol), phenol (3.64 g, 38.7 mmol), and triphenylphosphine (6.77 g, 25.8 mmol) in DCM (50 mL) was added a solution of diisopropyl azodicarboxylate (5.22 g, 25.8 mmol) in toluene (30 mL). After stirring at room temperature for 60 hours it was diluted with ether and the solution was extracted with aqueous 3N NaOH. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The intermediate tert-butyl (R)-2-(phenoxymethyl)pyrrolidine-1-carboxylate was obtained from the residue by column chromatography (silica gel, cHex/EtOAc 29:1); yield: 1.82 g (51%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09226929B2uspto-grants-2016_01