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Pempidine → Ethyl 3-phenylprop-2-enoate

HRID 1156449
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HRID 1156449 반응식
C(N([CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])CCCCCCCC)CCCCCCC.C(C(CC[CH2:49][CH3:50])CN(CC(CC)CCCC)CC(CC)CCCC)C.C(N(C1CCCCC1)C1CCCCC1)C.C(N(C(C)C)C(C)C)C.CN1C(C)(C)CCCC1(C)C.[C:86]([O-:89])(=[O:88])C.[Li+].C([O-])(=O)C.C[N+](C)(C)CC1C=CC=CC=1>C(N(CC)CC)C>[C:86]([O:89][CH2:49][CH3:50])(=[O:88])[CH:25]=[CH:24][C:23]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

9

반응물 7

HCID 6603PempidineHCID 14227TrioctylamineHCID 23563N-EthyldicyclohexylamineHCID 81531DiisopropylethylamineHCID 102705Tri(2-ethylhexyl)amineHCID 3474584Lithium acetateHCID 13086341Benzyltrimethylammonium acetate

생성물

1
HCID 7649Ethyl 3-phenylprop-2-enoate

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

The procedure described in Example 1 is repeated, except that 0.03125 mol of one of the bases tri-n-octylamine, tris-(2-ethylhexyl)-amine, ethyl-dicyclohexylamine, triethylamine, ethyl-diisopropylamine, N-methyl-2,2,6,6-tetramethylpiperidine, lithium acetate and trimethyl-benzylammonium acetate is used in place of 0.03125 mol of tri-n-butylamine. After working up as described in Example 1, ethyl cinnamate is obtained in comparably good yields.

출처 및 근거

ORD 기록
ord-e511e4f9f090421ca5ee66ff077b40fb
출처 데이터셋
uspto-grants-1982_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04335054

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