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

HRID 1447096
ノート
印刷プレビュー

反応式

HRID 1447096 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 3301EthylenediamineHCID 7170Ethyl benzoylacetate

生成物 1

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

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

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.

後処理

  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.)

出典と根拠

ORDレコード
ord-798e8bb35365449f84679de6952f2da2
出典データセット
uspto-grants-1982_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04315860

反応ノート

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