Sodium Bicarbonate → (4-Methoxymethylene-cyclohexyl)-methyl-carbamic acid benzyl ester

HRID 1743779노트

반응식

HRID 1743779 반응식
[Cl-].[CH3:2][O:3][CH2:4][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.CC(C)([O-])C.[K+].[CH2:30]([O:37][C:38](=[O:48])[N:39]([CH3:47])[CH:40]1[CH2:45][CH2:44][C:43](=O)[CH2:42][CH2:41]1)[C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1.C([O-])(O)=O.[Na+]>C1COCC1>[CH2:30]([O:37][C:38](=[O:48])[N:39]([CH:40]1[CH2:45][CH2:44][C:43](=[CH:2][O:3][CH3:4])[CH2:42][CH2:41]1)[CH3:47])[C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1

참가 물질

6

반응 조건

온도
-10 °C

실험 절차

A suspension of 749.88 g (2187.5 mmol) (methoxymethyl)triphenylphosphonium chloride in 2.5 l THF was cooled (−10° C.) and deprotonated with 245.5 g (2187.5 mmol) potassium t-butoxide. The dark red solution was stirred at 0–5° C. for 0.5 h, cooled (−20° C.) and 457.32 g (261.33 mmol) of Methyl-(4-oxo-cyclohexyl)-carbamic acid benzyl ester in 1.25 l THF were dropped in (1.25 h). After 1.3 h at RT, the reaction was treated with 1.75 l aqueous 1M NaHCO3 and stirred for 45 min. The phases were separated, the aqueous phase was extracted with TBME (700 ml), the organic phase was dried (Na2SO4), filtered and evaporated. The residue was suspended in hexane (5 l), cooled (0° C.), filtered and evaporated to give 495.2 g (98%) of (4-Methoxymethylene-cyclohexyl)-methyl-carbamic acid benzyl ester, MS: 289 (M).

후처리

  1. additionwere dropped in (1.25 h)
  2. waitAfter 1.3 h at RT
  3. stirringstirred for 45 min
  4. customThe phases were separated
  5. extractionthe aqueous phase was extracted with TBME (700 ml)
  6. dry with materialthe organic phase was dried (Na2SO4)
  7. filtrationfiltered
  8. customevaporated
  9. temperaturecooled (0° C.)
  10. filtrationfiltered
  11. customevaporated

출처 및 근거

ORD 기록
ord-a40efb8c5c0946debe0332b2e391e2d1
출처 데이터셋
uspto-grants-2006_03
특허 번호
US07012077B2

반응 노트

불러오는 중…