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Hydrochloric Acid → Bisphenol B

HRID 1583470
ノート
印刷プレビュー

反応式

HRID 1583470 の反応式
C1(O)C=CC=CC=1.SCC(O)=O.[OH:13][C:14]1[CH:19]=[CH:18][C:17]([C:20]([C:27]2[CH:32]=[CH:31][C:30]([OH:33])=[CH:29][CH:28]=2)([CH2:22][CH2:23]C(C)C)[CH3:21])=[CH:16][CH:15]=1.Cl>CC(=O)CC>[OH:13][C:14]1[CH:15]=[CH:16][C:17]([C:20]([C:27]2[CH:28]=[CH:29][C:30]([OH:33])=[CH:31][CH:32]=2)([CH2:22][CH3:23])[CH3:21])=[CH:18][CH:19]=1
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 996PhenolHCID 1133Thioglycolic AcidHCID 219104174,4'-(5-Methylhexane-2,2-diyl)diphenol

生成物 1

HCID 66166Bisphenol B

試薬・触媒・溶媒 1

HCID 6569Methyl Ethyl Ketone溶媒

実験手順

In a procedure substantially like that of Example 1, a mixture of 60 grams of phenol and 8 grams of 2-butanone was reacted in the presence of 1 ml. of mercaptoacetic acid (a catalyst used in place of the octanethiol of Example 1) and 40 ml. of concentrated hydrochloric acid. The Parr bomb and gaseous nitrogen were not used in this procedure. The reaction temperature was about 55° C. The crude reaction product was recrystallized from benzene to yield 5.2 grams of the title compound, which was dried overnight at about 95° C.

後処理

  1. customwas reacted in the presence of 1 ml
  2. customwas about 55° C
  3. customThe crude reaction product
  4. customwas recrystallized from benzene

出典と根拠

ORDレコード
ord-2fddf86af2a24c489f5aa01bfce92a35
出典データセット
uspto-grants-1985_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04551739

反応ノート

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