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Nicotinic Acid → Nicotinoyl chloride

HRID 5011
ノート
印刷プレビュー

反応式

HRID 5011 の反応式
[C:1]([OH:9])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[N:4][CH:3]=1.S(Cl)([Cl:12])=O.C(C1C=CC(OCCCCO)=CC=1)(C)(C)C>ClCCl>[C:1]([Cl:12])(=[O:9])[C:2]1[CH:7]=[CH:6][CH:5]=[N:4][CH:3]=1
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 938Nicotinic AcidHCID 24386Thionyl ChlorideHCID 133137374-(4-Tert-butylphenoxy)butan-1-OL

生成物 1

HCID 82604Nicotinoyl chloride

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

Nicotinoyl chloride was prepared by treating 100 g (0.81 mole) of nicotinic acid with 280 ml of thionyl chloride at reflux for two hours. The excess thionyl chloride was removed in vacuo and the crystalline acid chloride hydrochloride was suspended in 500 ml of dichloromethane. To the stirred mixture was added 66 g (0.30 mole) of 4-p-t-butylphenoxy-1-butanol dissolved in 400 ml of dichloromethane. After forty-eight hours the mixture was washed with one liter of saturated sodium bicarbonate. The dichloromethane solution was dried over magnesium sulfate and evaporated to a syrupy residue. The material was chromatographed on 1 kg of silica gel with elution by dichloromethane-methanol, 96:4, to afford 43.8 g (45%) of the nicotinate ester as an oil. The hydrobromide salt was prepared by treatment of a solution of 43.8 g in 800 ml of ethyl acetate with 30 ml of 4.5N hydrogen bromide in ether. The precipitate was collected, washed with pentane and dried, m.p. 132°-133° C.

後処理

  1. temperatureat reflux for two hours
  2. customThe excess thionyl chloride was removed in vacuo
  3. washAfter forty-eight hours the mixture was washed with one liter of saturated sodium bicarbonate
  4. dry with materialThe dichloromethane solution was dried over magnesium sulfate
  5. customevaporated to a syrupy residue
  6. customThe material was chromatographed on 1 kg of silica gel with elution by dichloromethane-methanol, 96:4

出典と根拠

ORDレコード
ord-d238f04b14bc48fe99e1c99449a0250c
出典データセット
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05242936

反応ノート

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