反応 #987047

ord-f47c460ec7e348ac82cab9f315f3f4cf

反応方程式

CCCCCCNCc1ccccc1
N-hexylbenzylamine
O=C(O)CCc1ccc(O)cc1
3-(4-hydroxyphenyl)propionic acid
On1nnc2ccccc21
HOBT
CN(C)C(On1nnc2ccccc21)=[N+](C)C.F[B-](F)(F)F
TBTU
CCN(C(C)C)C(C)C
DIPEA
CCCCCCN(Cc1ccccc1)C(=O)CCc1ccc(O)cc1
desired product
収率 71.4%
CCCCCCN(Cc1ccccc1)C(=O)CCc1ccc(O)cc1
N-benzyl-N-hexyl-3-(4-hydroxyphenyl)propanamide
収率 71.4%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度the mixture was cooled
  2. 2
    その他evaporated
  3. 3
    その他The resulting mixture was partitioned between ethyl acetate and sodium hydrogencarbonate aqueous solution (sat.)
  4. 4
    抽出The aqueous portion was extracted with ethyl acetate
  5. 5
    乾燥the combined organic extracts dried with magnesium sulphate
  6. 6
    その他evaporated

実験手順

N-hexylbenzylamine (0.6 g, 3.136 mmol) and 3-(4-hydroxyphenyl)propionic acid (0.52 g 3.136 mmol) were mixed in DMF (10 ml) and the mixture was cooled. HOBT (0.424 g, 3.136 mmol) and the TBTU (1 g, 3.136 mmol) reagent were added followed by DIPEA (1.216 g, 9.409 mmol). The mixture was stirred at room temperature overnight and then evaporated. The resulting mixture was partitioned between ethyl acetate and sodium hydrogencarbonate aqueous solution (sat.). The aqueous portion was extracted with ethyl acetate and the combined organic extracts dried with magnesium sulphate and then evaporated. Chromatography of the residue on a column (ISOLUTE® SI, 5 g/25 ml) using ethyl acetate/heptane (10:90, then 25:75) as eluant gave 760 mg the desired product, yield 71%.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07355069B2uspto-grants-2008_04