Methanol → 1-(2-Penten-1-yl)-2-naphthol

HRID 51171

反応式

HRID 51171 の反応式
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[OH:11].CO.[CH:14]1[CH2:18][CH:17]=[CH:16][CH:15]=1.C1COCC1>CC(CC(C)=O)C>[CH2:16]([C:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[OH:11])[CH:15]=[CH:14][CH2:18][CH3:17]

参加物

6

反応物 4

HCID 887Methanol2 回HCID 7612CyclopentadieneHCID 8028TetrahydrofuranHCID 86632-Naphthol

生成物 1

HCID 698872381-(2-Penten-1-yl)-2-naphthol

試薬・触媒・溶媒 1

HCID 7909Methyl Isobutyl Ketone溶媒

実験手順

Into a 2-liter flask having a stirrer, a condenser and a thermometer, 144 g of 2-naphthol, 200 g of methanol and 40 g of PTS were introduced, and a solution of mixture of 66 g of cyclopentadiene and 60 g of methanol was added dropwise over a period of 3 hours while stirring the mixture at room temperature, followed by further stirring for 4 hours at room temperature. To the reaction solution thus obtained, THF and MIBK were added, and the resultant solution was washed with 200 ml of an aqueous 10% sodium hydroxide solution five times, and thereafter further washed with water until it turned neutral, followed by removal of the solvent using an evaporator. The results of analysis by GPC thereof are shown in FIG. 11. Its yield determined by GPC was 90% (area ratio). An NMR spectrum of the 1-(2-penten-1-yl)-2-naphthol obtained is shown in FIG. 12.

後処理

  1. customInto a 2-liter flask having
  2. additionwas added dropwise over a period of 3 hours
  3. stirringby further stirring for 4 hours at room temperature
  4. customTo the reaction solution thus obtained
  5. washthe resultant solution was washed with 200 ml of an aqueous 10% sodium hydroxide solution five times
  6. washfurther washed with water until it
  7. customfollowed by removal of the solvent
  8. customan evaporator
  9. customThe results of analysis by GPC
  10. customIts yield

出典と根拠

ORDレコード
ord-6f961dfb283f4d78b6133c6ade4457f0
出典データセット
uspto-grants-2004_03
特許番号
US06713589B2

関連ノート

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