HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 2,3-Dimethyl-2-hydroxymethyl-pent-4en-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 1,3-Propanediol, 2-methyl-2-(1-methylpropyl)- | HCID 98076 | — |
| Reactant | 2,3-Dimethylpent-4-enal | HCID 110697 | — |
| Product | 2,3-Dimethyl-2-hydroxymethyl-pent-4en-ol | HCID 20349238 | — |
Reaction Steps
I have now found a novel method for producing mebutamate diol which includes the process steps of reacting crotyl alcohol and allyl chloride to produce a mixture of isomers of allyl crotyl ether, heating said crotyl ether to produce 2,3-dimethyl-pent-4en-aldehye. The aldehyde is then converted to 2-methyl-2-(sec butyl)-1, 3-propanediol by reacting 2,3-dimethyl-pent-4en-aldehyde and formaldehyde to produce 2,3-dimethyl-2-hydroxymethyl-pent-4en-ol and subsequently hydrogenating the said alcohol in the presence of a catalyst to produce 2-methyl-2-(sec butyl)-1,3-propanediol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04190607 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-8143118e4cdb4b3c9f15d08d73cf9747 |
| Source note | uspto-grants-1980_02 |