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Ethylenediamine → 7-Phenyl-1,2,3,4-tetrahydro-5H-1,4-diazepin-5-one

HRID 1447096
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HRID 1447096 반응식
[C:1]([CH2:9][C:10]([O:12]CC)=O)(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:15]([NH2:18])[CH2:16][NH2:17]>O>[C:2]1([C:1]2[NH:18][CH2:15][CH2:16][NH:17][C:10](=[O:12])[CH:9]=2)[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 3301EthylenediamineHCID 7170Ethyl benzoylacetate

생성물 1

HCID 128346207-Phenyl-1,2,3,4-tetrahydro-5H-1,4-diazepin-5-one

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A solution of 192 g. (1 mol) of ethyl benzoylacetate in mixed xylenes (total volume 400 ml.) was added dropwise over a 1 hour period to a solution of 60 g. (67 ml.; 1 mol) of ethylenediamine in 1 l. of mixed xylenes refluxing under nitrogen. The reaction mixture was then refluxed for an additional hour after which the water was azeotroped off. The solvent was then distilled off over a 2 hour period and the resulting reaction product was allowed to stand at room temperature. The crystalline material formed was isolated by filtration, washed several times with chloroform and dried to obtain the crystalline product (59 g.). m.p. 207°-210° C. Lit. Ried et al., Chem. Ber. 87, 1811-1814 (1954), m.p. 209°-210° C.; Hofmann et al., J. Org. Chem. 27, 3565-3568 (1962), m.p. 206°-209° C.

후처리

  1. customwas azeotroped off
  2. distillationThe solvent was then distilled off over a 2 hour period
  3. customthe resulting reaction product
  4. customto stand at room temperature
  5. customThe crystalline material formed
  6. customwas isolated by filtration
  7. washwashed several times with chloroform
  8. customdried
  9. customto obtain the crystalline product (59 g.)

출처 및 근거

ORD 기록
ord-798e8bb35365449f84679de6952f2da2
출처 데이터셋
uspto-grants-1982_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04315860

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