Succinic Acid → Bis[(4-methylcyclohex-3-en-1-yl)methyl] butanedioate

HRID 33609

反応式

HRID 33609 の反応式
[CH3:1][C:2]1[CH2:7][CH2:6][CH:5]([CH2:8][OH:9])[CH2:4][CH:3]=1.[C:10]1([CH3:16])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[C:17]([OH:24])(=O)[CH2:18][CH2:19][C:20]([OH:22])=[O:21].O.[C:26]1(C)C(S(O)(=O)=O)=CC=CC=1>O>[CH3:1][C:2]1[CH2:7][CH2:6][CH:5]([CH2:8][O:9][C:17](=[O:24])[CH2:18][CH2:19][C:20]([O:22][CH2:16][CH:10]2[CH2:15][CH2:14][C:13]([CH3:26])=[CH:12][CH2:11]2)=[O:21])[CH2:4][CH:3]=1

参加物

6

反応物 4

HCID 1110Succinic AcidHCID 1140TolueneHCID 5646723-Cyclohexene-1-methanol, 4-methyl-HCID 124969952-Methylbenzenesulfonic acid hydrate

生成物 1

HCID 69305714Bis[(4-methylcyclohex-3-en-1-yl)methyl] butanedioate収率 90%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Added to 284 g (being 2 mol) of 4-methyl-3-cyclohexenylmethanol and one liter toluene solution containing 10 g (being 1 mol) of succinic acid anhydrate, was 5 g of toluenesulfonic acid monohydrate, and allowed to react for 8 hours at 110-120° C., while any generated water was removed using a water separating apparatus. After the reacted solution was washed with sodium bicarbonate water, distillation under reduced pressure was conducted to remove any toluene. The residual crude product was distilled under reduced pressure to obtain the objective compound. The yield was 90%.

後処理

  1. customwas removed
  2. washAfter the reacted solution was washed with sodium bicarbonate water, distillation under reduced pressure
  3. customto remove any toluene
  4. distillationThe residual crude product was distilled under reduced pressure
  5. customto obtain the objective compound

出典と根拠

ORDレコード
ord-d8a7ba29005c42e5a62be1bcbb4d3711
出典データセット
uspto-grants-2008_09
特許番号
US07429622B2

関連ノート

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