반응 #95495

ord-5ad60d3a74f64df8b09f907777fdb700

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척Thereafter, the mixture is successively washed with 10% sodium hydroxide
  2. 2
    세척washed with water
  3. 3
    기타dried
  4. 4
    농축concentrated under vacuum
  5. 5
    기타leaving a brownish oil

실험 절차

A mixture of 0.8 g of 6-chloro-1-(2-chlorophenyl)-1'-methylspiro[indoline-3,4'-piperidine], free base of Example 28, and 0.5 g of phenyl chloroformate in 20 ml of methylene chloride is stirred at ambient temperature for 16 hours. Thereafter, the mixture is successively washed with 10% sodium hydroxide, washed with water, dried and concentrated under vacuum leaving a brownish oil. The oil is passed through an alumina column, ether eluant, providing a colorless gum of 6-chloro-1-(2-chlorophenyl)-1'-phenoxycarbonylspiro[indoline-3,4'-piperidine]. IR and NMR spectra confirm the assigned structure.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04345081uspto-grants-1982_08