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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
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Phenothiazine → 1,4-Butanediol

HRID 127143
ノート
印刷プレビュー

反応式

HRID 127143 の反応式
CC1C(=CC(=CC=1)N=C=O)N=[C:5]=[O:6].[CH:14]1[C:27]2NC3C(=CC=CC=3)SC=2C=C[CH:15]=1.[C:28]([O:32]CCO)(=O)[CH:29]=[CH2:30]>>[CH2:5]([OH:6])[CH2:30][CH2:29][CH2:28][OH:32].[CH2:15]([OH:6])[CH2:14][CH2:27][CH2:30][CH2:29][CH2:28][OH:32]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 7108PhenothiazineHCID 11443Toluene 2,4-DiisocyanateHCID 131652-Hydroxyethyl acrylate

生成物 2

HCID 80641,4-ButanediolHCID 123741,6-Hexanediol

実験手順

87 grams (0.5 mol) of toluene diisocyanate and 0.027 g of phenothiazine are placed in a 500 cm3 reactor under a nitrogen atmosphere. The temperature is kept at between 48° and 50° C. and 58 g, that is to say 0.5 mol, of freshly distilled hydroxyethyl acrylate are added in the course of two hours. When the introduction is complete, the mixture is stirred for a further 3 hours at the same temperature and 223 g, that is to say 0.25 mol, of an aliphatic polycarbonate-diol are then added, the latter having a molecular weight of 890 and being obtained by the phosgenation of a mixture of butane-1,4-diol and hexane-1,6-diol in proportions which are such that the resulting polycarbonate is equivalent to a mixture of 50% by weight of a polycarbonate obtained from hexane-1,6-diol by itself and 50% by weight of a polycarbonate obtained from butane-1,4-diol by itself. The reaction is allowed to proceed for 3 hours at 50° C. A few drops of methanol are added in order to neutralise any free isocyanate groups which could have remained.

後処理

  1. customis kept at between 48° and 50° C.

出典と根拠

ORDレコード
ord-bd9f356bbe22476cb31d322ecfae0893
出典データセット
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04255243

反応ノート

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