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Salicylaldehyde → cis-5-(Methoxycarbonyl)piperidine-2-carboxylic Acid

HRID 1728414
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HRID 1728414 반응식
[NH:1]1[CH2:6][C@H:5]([C:7]([O:9][CH3:10])=[O:8])[CH2:4][CH2:3][C@@H:2]1[C:11]([O:13]C)=[O:12].C(=O)C1C(=CC=CC=1)O>C(O)(=O)C>[CH3:10][O:9][C:7]([C@H:5]1[CH2:6][NH:1][C@@H:2]([C:11]([OH:13])=[O:12])[CH2:3][CH2:4]1)=[O:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6998SalicylaldehydeHCID 13413095HCID 13413095, 화합물

생성물 1

HCID 21782947cis-5-(Methoxycarbonyl)piperidine-2-carboxylic Acid

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
100 °C

실험 절차

Dimethyl cis-piperidine-2,5-dicarboxylate (112 g, 0.56 mol), salicylaldehyde (3 ml, 0.056 mol) and glacial acetic acid (600 ml) were combined and the resulting mixture heated at about 100° C. for 60 hours. The mixture was cooled, than stripped in vacuo to a thick oil from which 61.7 g (59%) of title products crystallized upon stirring with 800 ml of isopropyl alcohol. Product ratio was determined by 1H-NMR (D2O, 300 MHz), a peak at 3.13 ppm (t, 1H, J=14.5 Hz) being diagnostic of trans, and a peak at 3.33 ppm (dd, 1H) being diagnostic of cis.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperatureThe mixture was cooled
  2. customcrystallized

출처 및 근거

ORD 기록
ord-5d8161722ae64615837a13d351cbb5aa
출처 데이터셋
uspto-grants-1994_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05326874

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