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HRID 36402作成日:2026年10月24日

Acetic Acid → Oxane-4-carboxylic acid

https://huagongshe.com/ja/reaction/36402

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物MethanolHCID 887—
反応物WaterHCID 962—
反応物O-XyleneHCID 7237—
生成物Oxane-4-carboxylic acidHCID 219302—
生成物3-(2-Hydroxyethyl)butyrolactoneHCID 9877372—
生成物3-(2-Methoxyethyl)butyrolactoneHCID 15792967—
生成物3-(2-Acetoxyethyl)butyrolactoneHCID 19938662—

反応手順

100 parts of bottom product (7) from the first column (1) are passed into the second column (2) with 40 theoretical plates. 0.1 l of xylene (isomer mixture) is added as water entrainer and is returned (10) via line 8 and a phase separator (3) continuously into the column. With a distillate temperature of 28° C., a distillate pressure of 70 mbar and a reflux ratio of 1.6, 23 parts of overhead product (9) of the composition 80.1% by weight of water, 11.2% by weight of acetic acid, 3.3% by weight of methanol, 1.8% by weight of ester of tetrahydropyran-4-carboxylic acid and 44 parts of bottom product (12) with the composition 0.1% by weight of ester of tetrahydropyran-4-carboxylic acid, 10.7% by weight of 3-spirocyclopropylbutyrolactone, 28.9% by weight of 3-(2-methoxyethyl)butyrolactone, 6.1% by weight of 3-(2-hydroxyethyl)butyrolactone and 15.1% by weight of 3-(2-acetoxyethyl)butyrolactone are obtained. At 108° C., 33 parts of side stream (11) with the composition 99.5% by weight of ester of tetrahydropyran-4-carboxylic acid are removed at plate 27.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05414097
出典データセットuspto-grants-1995_05
ORD IDord-6d5fb5ec88a04b0cbeaba1bc9c75d4a5
出典メモuspto-grants-1995_05