Diethyl Ether → 4-Carbobenzoxyoxybenzoic acid 1-methylbutyl ester

反応式

[CH2:1]1[CH2:5]OC[CH2:2]1.C(N([CH2:11][CH3:12])CC)C.[C:13]([O:23][C:24]1[CH:32]=[CH:31][C:27]([C:28](Cl)=[O:29])=[CH:26][CH:25]=1)([O:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:14].CC[O:35]CC>>[CH3:2][CH:1]([O:29][C:28](=[O:35])[C:27]1[CH:31]=[CH:32][C:24]([O:23][C:13]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[O:14])=[CH:25][CH:26]=1)[CH2:5][CH2:11][CH3:12]

参加物

反応物 4

HCID 3283Diethyl Ether

HCID 8028Tetrahydrofuran2 回

HCID 8471Triethylamine

HCID 197340544-Carbobenzoxyoxybenzoyl chloride

生成物 1

HCID 542047674-Carbobenzoxyoxybenzoic acid 1-methylbutyl ester収率 13%

実験手順

A THF solution of 0.1 mole of (L)-(-)-2-pentanol and 0.1 mole of triethylamine was stirred t 0° C., and a THF solution of 0.12 mole of 4-carbobenzoxyoxybenzoyl chloride was added dropwise. The temperature was returned to the room temperature slowly, and stirring was carried out for 8 hours. After the reaction, the reaction solution was ether extracted, dried, and concentrated, then purified by column chromatography, to obtain 4.4 g of 4-carbobenzoxyoxybenzoic acid 1-methylbutyl ester. (yield: 13%)