反応 #438275

ord-38fe20f6332d4c4e924b82cd75dd348c

反応方程式

O=S(=O)(Cl)c1ccccc1
Benzenesulfonyl chloride
COC(=O)CCCCCN.Cl
methyl 6-aminohexanoate hydrochloride
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
COC(=O)CCCCCNS(=O)(=O)c1ccccc1
title compound
COC(=O)CCCCCNS(=O)(=O)c1ccccc1
6-Benzenesulfonylaminohexanoic acid methyl ester

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出the product was extracted with ethyl acetate (30 ml)
  2. 2
    乾燥The extract was dried (Na2SO4) and solvents
  3. 3
    その他were removed under reduced pressure
  4. 4
    その他The product was chromatographed on silica gel with ethyl acetate-hexane (1:2) as eluent

実験手順

Benzenesulfonyl chloride (92a) (0.88 g, 5.0 mmol) was added to the mixture of methyl 6-aminohexanoate hydrochloride (91) (1.82 g, 10 mmol) in acetonitrile (10 ml) and sodium carbonate (2.6 g, 24.6 mmol) in water (10 ml). The mixture was stirred for 6 hours at ambient temperature, and the product was extracted with ethyl acetate (30 ml). The extract was dried (Na2SO4) and solvents were removed under reduced pressure. The product was chromatographed on silica gel with ethyl acetate-hexane (1:2) as eluent. The title compound was obtained as oil (1.28 g, 90%). 1H NMR δH (90 MHz, DMSO-d6) δ: 0.90–1.63 (6H, m, CH2); 2.21 (2H, t, J=7.0 Hz, CH2); 2.71 (2H, q, J=6.0 Hz, CH2N); 3.58 (3H, s, CH3); 7.40–7.72 (3H, m, C6H3); 7.72–7.89 (2H, m, C6H2).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07183298B2uspto-grants-2007_02