反応 #1483096

ord-409e2acf49cc4982802955bb3c65c021

反応方程式

Cc1ccc(S(=O)(=O)O)cc1
pTSA
NC(Cc1ccccc1)C(=O)O
DL-phenylalanine
CCCCCCCCCCC(C)O
dodecanol 2
CCCCCCCCCCCCOC(=O)C(N)Cc1ccccc1
39
収率 99.1%
CCCCCCCCCCCCOC(=O)C(N)Cc1ccccc1
Dodecyl 2-amino-3-phenylpropanoate
収率 99.1%

試薬

なし

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The temperature of the reaction mixture was slowly raised
  2. 2
    温度to reflux temperature
  3. 3
    その他the water was separated azeotropically The reaction mixture
  4. 4
    濃縮The reaction mixture was concentrated under vacuum
  5. 5
    洗浄washed with aqueous 5% Na2CO3 (3×50 mL)
  6. 6
    乾燥The organic layer was dried over Na2SO4
  7. 7
    濃縮concentrated under vacuum

実験手順

To a stirred solution of DL-phenylalanine 38 (5 g, 30.26 mmol) in toluene (100 mL) was added dodecanol 2 (5.08 g, 27.24 mmol) in one lot, followed by pTSA (6.33 g, 33.29 mmol). The temperature of the reaction mixture was slowly raised to reflux temperature, and the water was separated azeotropically The reaction mixture was monitored by TLC. The reaction mixture was concentrated under vacuum. The obtained residue was taken in ethyl acetate (200 mL) and washed with aqueous 5% Na2CO3 (3×50 mL) followed by brine solution. The organic layer was dried over Na2SO4 and concentrated under vacuum to afford crude 39 (9 g, yield: 89.1%) as a liquid.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08900625B2uspto-grants-2014_12