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N,N-Diethylaniline → Propan-2-yl (3-chloro-4-ethoxy-5-ethylphenyl)carbamate

HRID 2308732
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HRID 2308732 반응식
[CH2:1]([C:3]1[CH:4]=[C:5]([CH:7]=[C:8]([Cl:13])[C:9]=1[O:10][CH2:11][CH3:12])[NH2:6])[CH3:2].CCN(C1C=CC=CC=1)CC.Cl[C:26]([O:28][CH:29]([CH3:31])[CH3:30])=[O:27]>C1(C)C=CC=CC=1>[CH2:1]([C:3]1[CH:4]=[C:5]([NH:6][C:26](=[O:27])[O:28][CH:29]([CH3:31])[CH3:30])[CH:7]=[C:8]([Cl:13])[C:9]=1[O:10][CH2:11][CH3:12])[CH3:2]
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참가 물질

5

반응물 3

HCID 7061N,N-DiethylanilineHCID 7917Isopropyl chloroformateHCID 201875993-Ethyl-4-ethoxy-5-chloroaniline

생성물 1

HCID 13303908Propan-2-yl (3-chloro-4-ethoxy-5-ethylphenyl)carbamate수율 89%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

3-Ethyl-4-ethoxy-5-chloroaniline (1.9 g) and diethylaniline (1.5 g) were dissolved in toluene (20 ml). To the resultant solution was dropwise added isopropyl chloroformate (1.2 g) in 5 minutes under ice-cooling. After being allowed to stand at room temperature for 12 hours, the reaction mixture was poured into ice-water and extracted with toluene. The extract was washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography using toluene as the eluent to give isopropyl N-(3-ethyl-4-ethoxy-5-chlorophenyl)carbamate (Compound No. 53) (2.4 g) in a yield of 89%. M.P., 79°-80.5° C.

후처리

  1. customin 5 minutes
  2. temperaturecooling
  3. extractionextracted with toluene
  4. washThe extract was washed with water
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-5ebd424459dc4d049d4a43624337c9d3
출처 데이터셋
uspto-grants-1987_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04690946

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