ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Potassium Carbonate → HCID 20336751、化合物

HRID 1973513
ノート
印刷プレビュー

反応式

HRID 1973513 の反応式
[C:1]1([S:7]([O-:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Na+].C(=O)([O-])[O-].[K+].[K+].Br[CH2:18][CH:19]=[C:20]1[CH2:24][CH2:23][CH2:22][CH2:21]1>[I-].[Na+].CO>[C:20]1(=[CH:19][CH2:18][S:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)(=[O:9])=[O:8])[CH2:24][CH2:23][CH2:22][CH2:21]1
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

6

反応物 3

HCID 11430Potassium CarbonateHCID 2723840Benzenesulfinic acid, sodium saltHCID 12772662(2-Bromoethylidene)cyclopentane

生成物 1

HCID 20336751HCID 20336751、化合物収率 47.1%

試薬・触媒・溶媒 2

HCID 5238Sodium Iodide触媒HCID 887Methanol溶媒

反応条件

温度
20 °C

実験手順

22.3 gm of sodium phenyl sulfinate, 2.2 gm of potassium carbonate and 0.2 gm of sodium iodide were introduced into 50 cc of methanol. Then 23.6 gm of 1-bromo-2-cyclopentylidene-ethane were added at a temperature of about +10° C and under agitation and the reaction mixture was agitated for 2 hours at 20° C. Thereafter, the reaction mixture was poured into ice water and cooled to 0° C. The precipitate formed was isolated by vacuum filtering and dried under vacuum in the presence of potassium hydroxide to obtain 15 gm of (2-cyclopentylidene-ethyl)-phenyl sulfone having a melting point of 68° C. A sample of the product crystallized from isopropyl ether had a melting point of 68° C.

後処理

  1. temperaturecooled to 0° C
  2. customThe precipitate formed
  3. customwas isolated by vacuum
  4. filtrationfiltering
  5. dry with materialdried under vacuum in the presence of potassium hydroxide

出典と根拠

ORDレコード
ord-dd9c6c8f068e45e89f3af3ce476db394
出典データセット
uspto-grants-1976_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03997586

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート