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Hydrochloric Acid → Ethanol, 2-(2-(2-(2-mercaptoethoxy)ethoxy)ethoxy)-

HRID 2221128
ノート
印刷プレビュー

反応式

HRID 2221128 の反応式
N[C:2](N)=[S:3].[OH:5][CH2:6][CH2:7][O:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13][O:14][CH2:15]COS(C1C=CC(C)=CC=1)(=O)=O.[OH-].[Na+].Cl>C(O)C.O>[SH:3][CH2:2][CH2:15][O:14][CH2:13][CH2:12][O:11][CH2:10][CH2:9][O:8][CH2:7][CH2:6][OH:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 2723790ThioureaHCID 134560942-(2-(2-(2-Hydroxyethoxy)ethoxy)ethoxy)ethyl 4-methylbenzenesulfonate

生成物 1

HCID 10465720Ethanol, 2-(2-(2-(2-mercaptoethoxy)ethoxy)ethoxy)-

試薬・触媒・溶媒 1

HCID 19096565Water ethanol
溶媒

実験手順

A solution of thiourea (0.94 g, 12.35 mmol) and toluene-4-sulfonic acid 2-{2-[2-(2-hydroxy-ethoxy)-ethoxy]-ethoxy)-ethyl ester (4.09 g, 11.75 mmol) in absolute alcohol (32 ml) was heated to reflux under argon atmosphere for 24 h. The mixture was cooled and a solution of NaOH (1.23 g, 30.75 mmol) in 15 ml of ethanol/water (9:1, v/v) was added. Refluxing was continued for another 2.5 h under argon. The reaction mixture was then cooled to ambient temperature and acidified to pH 2 using concentrated hydrochloric acid and then concentrated under reduced pressure. The residue was purified by flash chromatography using ethyl acetate/absolute ethanol (10:1) to afford the product as a colourless oil. Yield 1.55 g (66%).

後処理

  1. temperatureto reflux under argon atmosphere for 24 h
  2. temperatureThe mixture was cooled
  3. temperatureRefluxing
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by flash chromatography

出典と根拠

ORDレコード
ord-adfdeea70bd842ddbb86d9fb687995e4
出典データセット
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07368474B2

反応ノート

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