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Sodium Hydroxide → 2-nitromethylenetetrahydro-2H-1,3-thiazine

HRID 1732090
ノート
印刷プレビュー

反応式

HRID 1732090 の反応式
[NH2:1][CH2:2][CH2:3][CH2:4][SH:5].[OH-].[Na+].Cl[C:9](Cl)(Cl)[CH2:10][N+:11]([O-:13])=[O:12]>CO>[N+:11]([CH:10]=[C:9]1[NH:1][CH2:2][CH2:3][CH2:4][S:5]1)([O-:13])=[O:12]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 14798Sodium HydroxideHCID 974361-Propanethiol, 3-amino-HCID 109541031,1,1-Trichloro-2-nitroethane

生成物 1

HCID 428532-nitromethylenetetrahydro-2H-1,3-thiazine収率 86.8%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒3 回

反応条件

温度
0 °C

実験手順

Into 50 ml of methanol was added 8.1 g of 1-amino-3-propanethiol, followed by stirring, to be completely dissolved therein. Then, the mixture was cooled to 0° C. While stirring the solution, about 1/3-aliquot of a solution of 5.0 g of caustic soda dissolved in 40 ml of methanol was added dropwise thereinto, and the remainder of about 2/3-aliquot of the solution and a solution of 5.4 g of 2,2,2-trichloro-1-nitroethane diluted in 20 ml of methanol were added dropwise slowly over 50 minutes, and the reaction was carried out for one hour. During the dropwise addition, the liquid temperature was maintained at lower than 10° C. (about 8° C.). After the reaction carried out for one hour, the procedure of the post-treatments as described in Example 1 was followed to obtain 4.20 g of tetrahydro-2-(nitromethylene)-1,3thiazine (yield: 86.8%).

後処理

  1. dissolutionto be completely dissolved
  2. stirringWhile stirring the solution
  3. additionwas added dropwise
  4. additionwere added dropwise slowly over 50 minutes
  5. additionDuring the dropwise addition
  6. temperaturethe liquid temperature was maintained at lower than 10° C. (about 8° C.)
  7. waitAfter the reaction carried out for one hour

出典と根拠

ORDレコード
ord-ebe362574f2d45e0a8ccd267266d9602
出典データセット
uspto-grants-1986_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04625025

反応ノート

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