HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Formaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1,4-Butanediol | HCID 8064 | — |
| Solvent | Water | HCID 962 | — |
| Product | Formaldehyde | HCID 712 | — |
| Product | Acetylene | HCID 6326 | — |
| Product | 1,4-Butanediol | HCID 8064 | — |
| Product | 2-Butyne-1,4-diol | HCID 8066 | — |
Reaction Steps
We have found that this object is achieved by a novel process in which tetrahydrofuran is prepared from an aqueous butane-1,4-diol solution by eliminating water in the aqueous phase at elevated temperatures, under superatmospheric pressure and in the presence of an acid, wherein a crude aqueous solution of butane-1,4-diol, obtained by reaction of acetylene with aqueous formaldehyde and catalytic hydrogenation of the resulting but-2-yne-1,4-diol solution, is, when starting with a crude alkaline aqueous solution, neutralized with sulfuric acid, acidified by adding phosphoric acid, and then heated at from 200° to 260° C. under superatmospheric pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04588827 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-12681aaa946b4dca9fa235e3d8627b76 |
| Source note | uspto-grants-1986_05 |