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Cinnamaldehyde, thiosemicarbazone → HCID 2772307、化合物

HRID 1856382
ノート
印刷プレビュー

反応式

HRID 1856382 の反応式
[CH:1](=[N:10][NH:11][C:12]([NH2:14])=[S:13])[CH:2]=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1>O>[NH2:14][C:12]1[S:13][C:1]([CH:2]=[CH:3][C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=2)=[N:10][N:11]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 2737765Cinnamaldehyde, thiosemicarbazone

生成物 1

HCID 2772307HCID 2772307、化合物収率 78.6%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A mixture of 70.0 g (0.35 m) of cinnamaldehyde thiosemicarbazone and 56.0 g (1.16 m) of ferric ammonium sulfate dodecahydrate was pulverized with a mortar and pestle and added portionwise to 1400 ml of hot water. The mixture was stirred at 60°-100° C. for 11/4 hr., during which time the color of the mixture changed from yellow-orange to dark red and much of the solid material went into solution. The mixture was filtered hot to yield 54.5 g of a brown granular product. The mother liquors were cooled under refrigeration and refiltered to give another 12.3 g of product. The crude product was pulverized and triturated twice with chloroform to remove the residual starting material and the dark brown impurities from the product, leaving 27.4 g of a beige microcrystalline powder. An additional 4.60 g of product was recovered by concentrating the chloroform filtrate. Total yield was 32.0 g (0.16 m), mp. 212°-214° C. (dec.). This procedure is novel and is of general utility for preparing these types of compounds. The novel procedure for this particular product is defined as:

後処理

  1. filtrationThe mixture was filtered hot

出典と根拠

ORDレコード
ord-1daf32051ab842d6865d0a050786bdaf
出典データセット
uspto-grants-1980_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04219475

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート