HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Butanediol → Formaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Butanediol | HCID 8064 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Formaldehyde | HCID 712 | — |
| Product | Acetylene | HCID 6326 | — |
| Product | 2-Butyne-1,4-diol | HCID 8066 | — |
Reaction Steps
Tetrahydrofuran is prepared from a crude alkaline aqueous solution of butane-1,4-diol, as obtained by reaction of acetylene with aqueous formaldehyde and catylytic hydrogenation of the resulting but-2-yne-1,4-diol solution by a process in which the alkaline solution is first neutralized with sulfuric acid and water is then eliminated in the liquid phase at from 200° to 260° C., under superatmospheric pressure and in the presence of phosphoric acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04588827 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-ebf11e2b76dc432091730c767df7a461 |
| Source note | uspto-grants-1986_05 |