홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Sodium Hydroxide → 4-(2-methylpyrimidin-5-yl)tetrahydro-2H-pyran-4-carboxylic acid

HRID 512188
노트
인쇄 미리보기

반응식

HRID 512188 반응식
[CH3:1][C:2]1[N:7]=[CH:6][C:5]([C:8]2([C:14]#N)[CH2:13][CH2:12][O:11][CH2:10][CH2:9]2)=[CH:4][N:3]=1.[OH-:16].[Na+].C[OH:19].O>>[CH3:1][C:2]1[N:7]=[CH:6][C:5]([C:8]2([C:14]([OH:19])=[O:16])[CH2:13][CH2:12][O:11][CH2:10][CH2:9]2)=[CH:4][N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 14798Sodium HydroxideHCID 22242641Methanol--water (1/1)HCID 867162154-(2-methylpyrimidin-5-yl)tetrahydro-2H-pyran-4-carbonitrile

생성물 1

HCID 867162164-(2-methylpyrimidin-5-yl)tetrahydro-2H-pyran-4-carboxylic acid수율 67%

반응 조건

온도
100 °C

실험 절차

A mixture of 4-(2-methylpyrimidin-5-yl)tetrahydro-2H-pyran-4-carbonitrile (5.5 g, 0.027 mol) in MeOH/H2O (60 mL, 1:1) was added NaOH (3.25 g, 0.081 mol) and heated to 100° C. overnight. The MeOH was removed in vacuo. The aqueous layer was extracted with EtOAc (2×30 mL) and the organic layers was discarded. The aqueous layer was adjusted pH to 2˜3 with 3N HCl and extracted with EtOAc (6×50 mL). The organic layer was dried over Na2SO4 and concentracted to give 4-(2-methylpyrimidin-5-yl)tetrahydro-2H-pyran-4-carboxylic acid (4.0 g, yield: 67%). 1H NMR (DMSO-d6 400 MHz): δ13.04 (br, 1H), 8.71 (s, 2H), 3.80-3.70 (m, 2H), 3.60-3.40 (m, 2H), 2.61 (s, 3H), 2.40-2.30 (m, 2H), 2.00-1.85 (m, 2H).

후처리

  1. customThe MeOH was removed in vacuo
  2. extractionThe aqueous layer was extracted with EtOAc (2×30 mL)
  3. extractionextracted with EtOAc (6×50 mL)
  4. dry with materialThe organic layer was dried over Na2SO4

출처 및 근거

ORD 기록
ord-fd7cbb7639c649efa97b617de9fede29
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09102591B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트