Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Methanol | HCID 887 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | O-Xylene | HCID 7237 | — |
| Produkt | Oxane-4-carboxylic acid | HCID 219302 | — |
| Produkt | 3-(2-Hydroxyethyl)butyrolactone | HCID 9877372 | — |
| Produkt | 3-(2-Methoxyethyl)butyrolactone | HCID 15792967 | — |
| Produkt | 3-(2-Acetoxyethyl)butyrolactone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05414097 |
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| Quelldatensatz | uspto-grants-1995_05 |
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| ORD ID | ord-6d5fb5ec88a04b0cbeaba1bc9c75d4a5 |
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| Quellennotiz | uspto-grants-1995_05 |
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