Acetic Acid → 4-(1,4-Dioxa-8-aza-spiro[4.5]dec-8-yl)-benzoic acid

HRID 1794798

반응식

HRID 1794798 반응식
C([O:3][C:4](=[O:21])[C:5]1[CH:10]=[CH:9][C:8]([N:11]2[CH2:20][CH2:19][C:14]3([O:18][CH2:17][CH2:16][O:15]3)[CH2:13][CH2:12]2)=[CH:7][CH:6]=1)C.[OH-].[Na+].C(O)(=O)C>CO>[O:15]1[C:14]2([CH2:19][CH2:20][N:11]([C:8]3[CH:9]=[CH:10][C:5]([C:4]([OH:21])=[O:3])=[CH:6][CH:7]=3)[CH2:12][CH2:13]2)[O:18][CH2:17][CH2:16]1

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 14798Sodium HydroxideHCID 12717439Ethyl 4-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)benzoate

생성물 1

HCID 159484254-(1,4-Dioxa-8-aza-spiro[4.5]dec-8-yl)-benzoic acid수율 99%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of 4-(1,4-dioxa-8-aza-spiro[4.5]dec-8-yl)-benzoic acid ethyl ester (14 g, 48.1 mmol) (Taylor, E. C., Skotnicki, J. S. Synthesis, 1981, 606) in methanol/tetrahydronfuran (1:1, 100 mL) and sodium hydroxide (2 N, 150 mL) was refluxed for 2 hours. After cooling to room temperature the solution was acidified by acetic acid and the solid which was formed was collected and dried to give the title compound as a white solid (12.5 g, 99%); 1H NMR (300 MHz, CDCl3) δ 1.67 (t, J=5.6 Hz, 4 H), 3.43 (t, J=5.6 Hz, 4 H), 3.92 (s, 4 H), 6.96 (d, J=9.0 Hz, 2 H), 7.75 (d, J=9.0 Hz, 2 H); MS (ES) m/z: 264.4 (MH+); HRMS Calcd. for C14H17NO4(M+): 263.1158. Found: 263.1160.

후처리

  1. temperaturewas refluxed for 2 hours
  2. customthe solid which was formed
  3. customwas collected
  4. customdried

출처 및 근거

ORD 기록
ord-ebfd3ada21c1440da59c9b17b96be69b
출처 데이터셋
uspto-grants-2006_04
특허 번호
US07022716B2

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