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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36402Erstellt: 23. Oktober 2026

Acetic Acid → Oxane-4-carboxylic acid

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktMethanolHCID 887—
EduktWaterHCID 962—
EduktO-XyleneHCID 7237—
ProduktOxane-4-carboxylic acidHCID 219302—
Produkt3-(2-Hydroxyethyl)butyrolactoneHCID 9877372—
Produkt3-(2-Methoxyethyl)butyrolactoneHCID 15792967—
Produkt3-(2-Acetoxyethyl)butyrolactoneHCID 19938662—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05414097
Quelldatensatzuspto-grants-1995_05
ORD IDord-6d5fb5ec88a04b0cbeaba1bc9c75d4a5
Quellennotizuspto-grants-1995_05