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3,4-dihydro-2H-pyran → Methyl 3-(2-tetrahydropyranyloxy)cyclohexanecarboxylate

HRID 1462921
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반응식

HRID 1462921 반응식
[OH:1][CH:2]1[CH2:7][CH2:6][CH2:5][CH:4]([C:8]([O:10][CH3:11])=[O:9])[CH2:3]1.[O:12]1[CH:17]=[CH:16][CH2:15][CH2:14][CH2:13]1>CCOCC.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>[O:12]1[CH2:17][CH2:16][CH2:15][CH2:14][CH:13]1[O:1][CH:2]1[CH2:7][CH2:6][CH2:5][CH:4]([C:8]([O:10][CH3:11])=[O:9])[CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 80803,4-dihydro-2H-pyranHCID 12209242Methyl 3-hydroxycyclohexane-1-carboxylate

생성물 1

HCID 13236238Methyl 3-(2-tetrahydropyranyloxy)cyclohexanecarboxylate수율 65.8%

시약·촉매·용매 2

HCID 521998p-Toluenesulfonic acid monohydrate촉매HCID 3283Diethyl Ether용매

실험 절차

To a solution of methyl 3-hydroxycyclohexanecarboxylate [J. Am. Chem. Soc., 70, 1898 (1948)] (61 g) in ether (500 ml), 2,3-dihydropyran (49 g) and p-toluenesulfonic acid monohydrate (1 g) were added. The mixture was stirred at room temperature for 6 hours and washed with water and dried (MgSO4). The ether was distilled off, and the oily residue was distilled under reduced pressure to give methyl 3-(2-tetrahydropyranyloxy)cyclohexanecarboxylate (61.5 g, 60.2%, b.p. 120°-123° C./0.3 mmHg).

후처리

  1. washwashed with water
  2. dry with materialdried (MgSO4)
  3. distillationThe ether was distilled off
  4. distillationthe oily residue was distilled under reduced pressure

출처 및 근거

ORD 기록
ord-cd85fc058c144124b41814cf05302224
출처 데이터셋
uspto-grants-1984_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04461902

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