HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857807Generated: October 27, 2026
Acetic Acid → 3-(Acetoxymethyl)tetrahydrofuran
https://huagongshe.com/reaction/1857807
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3-Methyltetrahydrofuran | HCID 98230 | — |
| Reactant | Tetrahydro-3-furanmethanol | HCID 139980 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(Acetoxymethyl)tetrahydrofuran | HCID 11217321 | — |
Reaction Steps
Process for the preparation of 3-methyltetrahydrofuran (3-MeTHF) by the steps comprising (1) contacting 3-(hydroxymethyl)tetrahydrofuran (3-HOMeTHF) with acetic acid at a temperature of about 120 to 210° C. in an esterification zone using apparatus which permits water to be removed from the esterification zone to produce 3-(acetoxymethyl)tetrahydrofuran (3-AcOMETHF); (2) heating the 3-AcOMETHF in a pyrolysis zone at a temperature in the range of about 380 to 510° C. for a about 1 to 10 seconds to convert the ester compound to 3-methyleneTHF; and (3) contacting the 3-methyleneTHF with hydrogen at a temperature of 25 to 100° C. and a pressure in the range of about 1 to 50 bar absolute in the presence of a hydrogenation catalyst selected from supported catalysts comprising about 1 to 10 weight percent palladium, platinum or rhodium deposited on a catalyst support material to convert the 3-methyleneTHF to 3-MeTHF.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06147233 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-c27dad19b6144067b7569a0b721d1f4a |
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| Source note | uspto-grants-2000_11 |
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