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Dicyclopropylmethylamine hydrochloride → HCID 178513036、化合物

HRID 1691771
ノート
印刷プレビュー

反応式

HRID 1691771 の反応式
Cl.[CH:2]1([CH:5]([NH2:9])[CH:6]2[CH2:8][CH2:7]2)[CH2:4][CH2:3]1.[C:10]([NH:12][C:13]([NH2:15])=[NH:14])#[N:11]>CCCCCCCCCC.C1(C)C=CC=CC=1>[CH:2]1([CH:5]([NH:9][C:10]([NH:12][C:13]([NH2:15])=[NH:14])=[NH:11])[CH:6]2[CH2:8][CH2:7]2)[CH2:4][CH2:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 16613886Dicyclopropylmethylamine hydrochlorideHCID 178418324HCID 178418324、化合物

生成物 1

HCID 178513036HCID 178513036、化合物収率 80.6%

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒2 回HCID 15600Decane溶媒

実験手順

1.6 g (10.8 mmol) of 1,1-dicyclopropylmethylamine hydrochloride were admixed with 0.91 g (10.8 mmol) of cyanoguanidine in a mixture of 6 ml of decane and 20 ml of toluene. The mixture was heated to a temperature of 140° C. for 5 h, in the course of which toluene distilled off. The flask contents were cooled to room temperature, then acetone was added. The precipitate was decanted off and freed of residual solvent under reduced pressure. 1.7 g of the crude product (purity approx. 80%) were obtained, which were used for the next synthesis stage without further purification.

後処理

  1. distillationdistilled off
  2. additionacetone was added
  3. customThe precipitate was decanted off

出典と根拠

ORDレコード
ord-c2353c719ba14b2f968d2c7799f3399e
出典データセット
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08153788B2

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