반응 #10444

ord-2c40f5f2214f4dffa7218b5f4c2a3986

반응 방정식

CC=C1CCN(C(=O)OCc2ccccc2)C1
3-ethylidenepyrrolidine-1-carboxylic acid benzyl ester
CC=C1CCN(C(=O)OCc2ccccc2)C1
3-Ethylidenepyrrolidine-1-carboxylic acid benzyl ester
O=C(OO)c1cccc(Cl)c1
3-chloroperoxybenzoic acid
O=S([O-])[O-].[Na+].[Na+]
sodium sulfite
CC1OC12CCN(C(=O)OCc1ccccc1)C2
title compound
수율 44.8%
CC1OC12CCN(C(=O)OCc1ccccc1)C2
2-Methyl-1-oxa-5-azaspiro[2,4]heptane-5-carboxylic acid benzyl ester
수율 44.8%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척The organic layer is washed with 5% sodium bicarbonate solution
  2. 2
    건조dried over Na2SO4
  3. 3
    기타evaporated
  4. 4
    기타The residue is purified by column chromatography (1:1 hexanes/ethyl acetate)

실험 절차

A solution of 3-ethylidenepyrrolidine-1-carboxylic acid benzyl ester (Example A8, 0.65 g, 2.8 mmol) and 3-chloroperoxybenzoic acid (0.86 g, 5 mmol) in dichloromethane (15 mL) is stirred at room temperature for 3 hours. The excess peracid is decomposed by the addition of 10% sodium sulfite. The organic layer is washed with 5% sodium bicarbonate solution, dried over Na2SO4 and evaporated. The residue is purified by column chromatography (1:1 hexanes/ethyl acetate) to afford the title compound (0.310 g). 1H NMR (200 MHz, CDCl3): δ 7.36–7.26 (m, 5H), 5.14 (s, 2H), 3.73–3.55 (m, 3H), 3.34 (d. 1H), 3.20–3.13 (m, 1H), 2.26–2.11 (m, 1H), 1.90–1.62 (m, 1H), 1.33 (d, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07094780B1uspto-grants-2006_08