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Carbon Disulfide → 2-(2-Isothiocyanatoethyl)thiophene

HRID 240825
ノート
印刷プレビュー

反応式

HRID 240825 の反応式
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][CH2:7][NH2:8].C(N(CC)CC)C.[C:16](=S)=[S:17].ClC(OCC)=O.[OH-].[Na+]>ClCCCl.O>[N:8]([CH2:7][CH2:6][C:2]1[S:1][CH:5]=[CH:4][CH:3]=1)=[C:16]=[S:17]
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

8

反応物 5

HCID 6348Carbon DisulfideHCID 8471TriethylamineHCID 10928Ethyl chloroformateHCID 14798Sodium HydroxideHCID 116521Thiopheneethanamine

生成物 1

HCID 101763092-(2-Isothiocyanatoethyl)thiophene

試薬・触媒・溶媒 2

HCID 11
1,2-Dichloroethane
溶媒
2 回
HCID 962Water溶媒

反応条件

温度
0 °C

実験手順

Thiopene ethylamine (4.60 mL, 39.31 mmol) and triethyl amine (5.00 mL, 39.31 mmol) were dissolved in 1,2-dichloroethane (25 mL), and the resulting mixture was cooled to 0° C. A solution of carbon disulfide (2.36 mL, 39.31 mmol) in 1,2-dichloroethane (50 mL) was added dropwise thereto over 15 min. The reaction mixture was allowed to warm to room temperature and re-cooled to 0° C., to which ethyl chloroformate (4.27 mL, 31.39 mmol) was added dropwise. The reaction mixture was stirred at room temperature for about 1-2 h, and water (150 mL) and aqueous 2N sodium hydroxide (75 mL) were sequentially added thereto. The resulting mixture was extracted with dichloromethane. The extract was washed with water and brine, dried over sodium sulfate, and concentrated, to obtain the yellow title compound in a liquid form (5.37 g, 80.75%).

後処理

  1. temperatureto warm to room temperature
  2. additionwas added dropwise
  3. extractionThe resulting mixture was extracted with dichloromethane
  4. washThe extract was washed with water and brine
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-d8688be4626044dc953fffbd628dbc8b
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08648111B2

反応ノート

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