HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrolein → 3,3-Diethoxy-1-propene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrolein | HCID 7847 | — |
| Reactant | 1,4-Butanediol | HCID 8064 | — |
| Reactant | Methylpropanediol | HCID 75103 | — |
| Product | 3,3-Diethoxy-1-propene | HCID 62477 | — |
Reaction Steps
U.S. Pat. Nos. 3,929,915, 3,963,754 and JP-A-Sho 61-39613 report a three-step process for preparing 1,4-butanediol which comprises reaction of acrolein with 2-methyl-1,3-propanediol under conventional conditions to produce acrolein acetal (2-vinyl-5-methyl-1,3-dioxane) (Reaction 1), hydroformylation of the acrolein acetal under conventional conditions to produce the corresponding aldehydes (Reaction 2), and hydrolysis and hydrogenation of the aldehyde of 2-vinyl-5-methyl-1,3-dioxane under conventional conditions to obtain a mixture of 1,4-butanediol and 2-methyl-1,3-propanediol (Reaction 3). ##STR4##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05606079 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-83b52f3aa2034f81b92e79b9ac835153 |
| Source note | uspto-grants-1997_02 |