Stannous Chloride → 4-Hydrazino-5,6,7,8-tetrahydro-1-naphthalenecarboxylic acid hydrochloride

HRID 1082

反応式

HRID 1082 の反応式
[N:1]([O-])=O.[Na+].[NH2:5][C:6]1[C:15]2[CH2:14][CH2:13][CH2:12][CH2:11][C:10]=2[C:9]([C:16]([OH:18])=[O:17])=[CH:8][CH:7]=1.[Cl:19][Sn]Cl>O.Cl>[ClH:19].[NH:5]([C:6]1[C:15]2[CH2:14][CH2:13][CH2:12][CH2:11][C:10]=2[C:9]([C:16]([OH:18])=[O:17])=[CH:8][CH:7]=1)[NH2:1]

参加物

6

反応物 3

HCID 24479Stannous ChlorideHCID 221117984-Amino-5,6,7,8-tetrahydronaphthalene-1-carboxylic acidHCID 23668193Sodium Nitrite

生成物 1

HCID 702454754-Hydrazino-5,6,7,8-tetrahydro-1-naphthalenecarboxylic acid hydrochloride収率 73.3%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒2 回HCID 962Water溶媒

反応条件

温度
-5 °C

実験手順

A solution of 0.26 g of NaNO2 in 1 ml of water is added to a solution, cooled to -5° C., of 0.73 g of 4-amino-5,6,7,8-tetrahydro-1-naphthalenecarboxylic acid in 10 ml of concentrated HCl. After one and a half hours of stirring at -5° C., a solution of 3.4 g of SnCl2 ·2H2O in 34 ml of concentrated HCl is added at -5° C. The mixture is stirred for 1 hour at RT and filtered, and the product is washed with concentrated HCl and dried under a stream of dry nitrogen to obtain 0.67 g of the expected hydrazine.

後処理

  1. stirringThe mixture is stirred for 1 hour at RT
  2. filtrationfiltered
  3. washthe product is washed with concentrated HCl
  4. customdried under a stream of dry nitrogen

出典と根拠

ORDレコード
ord-7bfae8fa5eb84c9b9f50ce2960b99ca7
出典データセット
uspto-grants-1998_03
特許番号
US05723483

関連ノート

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