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Water → 8-Methoxy-3,7-dimethyl-octa-1,6-dien-3-ol

HRID 437497
ノート
印刷プレビュー

反応式

HRID 437497 の反応式
[CH3:1][O:2][CH:3](C)[C:4]([CH3:11])=[CH:5][CH2:6][CH2:7][C:8](=[O:10])[CH3:9].[CH:13]([Mg]Cl)=[CH2:14].O>O1CCCC1>[CH3:1][O:2][CH2:3][C:4]([CH3:11])=[CH:5][CH2:6][CH2:7][C:8]([CH3:9])([OH:10])[CH:13]=[CH2:14]
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 962WaterHCID 53786798HCID 53786798、化合物HCID 178461836HCID 178461836、化合物

生成物 1

HCID 539177528-Methoxy-3,7-dimethyl-octa-1,6-dien-3-ol収率 85%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

141 g (0.9 mole) of 7-methoxy-6-methyl-oct-5-en-2-one are added to 1 mole of a 1.5 normal solution of vinyl-magnesium chloride in tetrahydrofuran, at below 20° C, in the course of one hour. After a further 2 hours' reaction, hydrolysis is carried out with 100 ml of water, whilst cooling with ice. After a homogeneous salt suspension has formed, the salt and the tetrahydrofuran solution are separated by filtering or centrifuging. The tetrahydrofuran is distilled off under reduced pressure and the reaction product which remains is purified by fractional distillation. 164 g of 8-methoxy-3,7-dimethyl-octa-1,6-dien-3-ol (yield 85%) are obtained. Boiling point 73°-75° C/0.01 bar; nD25 = 1.4676.

後処理

  1. customAfter a further 2 hours' reaction, hydrolysis
  2. temperaturewhilst cooling with ice
  3. customAfter a homogeneous salt suspension has formed
  4. customthe salt and the tetrahydrofuran solution are separated
  5. filtrationby filtering
  6. distillationThe tetrahydrofuran is distilled off under reduced pressure
  7. distillationthe reaction product which remains is purified by fractional distillation

出典と根拠

ORDレコード
ord-6664a19cec2f4dc6a0695b347a1f976c
出典データセット
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04031141

反応ノート

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