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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Octanoic Acid → 4-Cyanobenzaldehyde

HRID 1922334
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HRID 1922334 반응식
[O:1]1CCO[CH:2]1[C:6]1[CH:13]=[CH:12][C:9]([CH2:10][NH2:11])=[CH:8][CH:7]=1.C(O)(=O)CCCCCCC.C1CCC(N=C=NC2CCCCC2)CC1.C1C=CC2N(O)N=NC=2C=1>ClCCl>[C:10]([C:9]1[CH:12]=[CH:13][C:6]([CH:2]=[O:1])=[CH:7][CH:8]=1)#[N:11]
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참가 물질

6

반응물 4

HCID 379Octanoic AcidHCID 10868DicyclohexylcarbodiimideHCID 757711-HydroxybenzotriazoleHCID 10559254[4-(1,3-Dioxolan-2-yl)phenyl]methanamine

생성물 1

HCID 660424-Cyanobenzaldehyde수율 40%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

The 4-(1,3-dioxacyclopent-2-yl)benzylamine is condensed with octanoic acid in dichloromethane in the presence of a peptide coupling system consisting of DCC and HOBt according to a method already described (Ouari O.; Polidori A.; Pucci B.; Tordo P.: Chalier F. J. Org. Chem. 1999, 64, 3554-3556) and then the dioxolane protecting group is removed by treatment in a 1:1, v/v, acetic acid/water mixture. Compound 3 is subsequently purified by silica gel chromatography (eluent: cyclohexane/EtOAc, 6:4, v/v) to give a white powder with a yield of 40% from the 4-cyanobenzaldehyde.

후처리

  1. customthe dioxolane protecting group is removed by treatment in a 1:1, v/v, acetic acid/water mixture
  2. customCompound 3 is subsequently purified by silica gel chromatography (eluent: cyclohexane/EtOAc, 6:4, v/v)

출처 및 근거

ORD 기록
ord-06567bf4ccce44dfa8543fe72c56cd12
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08173843B2

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