HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 22164489, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 14495344 | HCID 14495344 | — |
| Product | HCID 22164489 | HCID 22164489 | 87% |
Reaction Steps
A 10 1 magnetic lift stirred autoclave is charged with 1,015 g of 2,3,3-trimethoxyprop-1-ene together with 3,000 g of tetrahydrofuran and 500 mg of Rh2 (COD)2Cl2 as hydroformylation catalyst. The oxo reaction is carried out under a pressure of 500 bar (CO/H2 =1:1) at 40° C. for 6 hours, at 60° C./550 bar for another 6 hours and at 80° C./600 bar for a further 6 hours. According to gas chromatography, this way of carrying out the reaction gives a conversion of 94%. The desired compound 3,4,4-trimethoxybutanal (bp=135° C./110 mbar) is obtained in the yield of 87% following fraction-ation. Preparation of methyl 2-methoxyacrylate
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04960954 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-d980a0fee8394500b686459609a61b05 |
| Source note | uspto-grants-1990_10 |