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Sulfur → 6-Butoxy-2-naphthoic acid

HRID 1638780
ノート
印刷プレビュー

反応式

HRID 1638780 の反応式
[CH2:1]([O:5][C:6]1[CH:15]=[C:14]2[C:9]([CH:10]=[C:11]([C:16]([OH:18])=[O:17])[CH2:12][CH2:13]2)=[CH:8][CH:7]=1)[CH2:2][CH2:3][CH3:4].[S]>C(OCC)C>[CH2:1]([O:5][C:6]1[CH:15]=[C:14]2[C:9](=[CH:8][CH:7]=1)[CH:10]=[C:11]([C:16]([OH:18])=[O:17])[CH:12]=[CH:13]2)[CH2:2][CH2:3][CH3:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 5362487SulfurHCID 146761917-Butoxy-1,2-dihydro-3-naphthoic acid

生成物 1

HCID 110211286-Butoxy-2-naphthoic acid

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

A mixture of 7-butoxy-1,2-dihydro-3-naphthoic acid (0.9 g) and powdery sulfur (0.25 g) is heated at 200°-210° C. for 35 minutes. After cooling, the mixture is dissolved in ethyl ether (200 ml). The solution is extracted with a 0.5N aqueous solution of sodium hydroxide. The aqueous layer is made acid with concentrated hydrochloric acid, and the precipitating crystals are collected by filtration. The crystals are dissolved in acetone, and insolubles are filtered off. The filtrate is concentrated under reduced pressure to allow crystals to precipitate. To the precipitates is added (100 ml), and the precipitates are collected by filtration to afford 6-butoxy-2-naphthoic acid

後処理

  1. temperatureis heated at 200°-210° C. for 35 minutes
  2. temperatureAfter cooling
  3. extractionThe solution is extracted with a 0.5N aqueous solution of sodium hydroxide
  4. filtrationthe precipitating crystals are collected by filtration
  5. dissolutionThe crystals are dissolved in acetone
  6. filtrationinsolubles are filtered off
  7. concentrationThe filtrate is concentrated under reduced pressure
  8. customto precipitate
  9. additionTo the precipitates is added (100 ml)
  10. filtrationthe precipitates are collected by filtration

出典と根拠

ORDレコード
ord-5a540c3f4ca048999365cff9d3d92094
出典データセット
uspto-grants-1989_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04880809

反応ノート

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