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2-Chlorobenzaldehyde → HCID 56616910, 화합물

HRID 1979801
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HRID 1979801 반응식
[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=O.[NH2:10][CH2:11][P:12]([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C([O:28]C(C)C)(C)C>C(O)C>[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=[N:10][CH2:11][P:12](=[O:28])([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 69962-ChlorobenzaldehydeHCID 7914Diisopropyl EtherHCID 20439053HCID 20439053, 화합물

생성물 1

HCID 56616910HCID 56616910, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매2회

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온도
50 °C

실험 절차

2.18 g. (0.015 mol) o-chlorobenzaldehyde is added dropwise to a solution of 3.5 g. (0.015 mol) aminomethyldiphenylphosphine in 150 ml. ethanol at ambient temperature. After evaporation of the solvent by heating to 50° C. under a slight vacuum, a clear yellow oil is obtained which is taken up hot in 50 ml. of a mixture of diisopropyl ether and ethanol (25/1 v/v). After cooling to 10° C., filtering and drying at 40° C. in vacuo, there are obtained 4.9 g. of crystals of the desired product; m.p. 89° C.

후처리

  1. customat ambient temperature
  2. customAfter evaporation of the solvent
  3. customa clear yellow oil is obtained which
  4. temperatureAfter cooling to 10° C.
  5. filtrationfiltering
  6. customdrying at 40° C. in vacuo, there
  7. customare obtained 4.9 g

출처 및 근거

ORD 기록
ord-a2787c4a073446309247945ac01731eb
출처 데이터셋
uspto-grants-1984_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04482718

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