HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429603Generated: October 30, 2026
3,3-Dimethoxybutan-2-ol → 3,3-Dimethoxy-2-butanone
https://huagongshe.com/reaction/429603
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,3-Dimethoxybutan-2-ol | HCID 102794 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 3,3-Dimethoxy-2-butanone | HCID 140871 | — |
Reaction Steps
Advantageous starting materials of the formula II are also compounds in which X is 2 alkoxy groups. These can be obtained very advantageously, even industrially, by the electrochemical process described in EP 460 451 B1. Thus, for example, 3,3-dimethoxy-2-butanol, which is particularly suitable for the preparation of diacetyl, is obtained by this process from 2-butanone (methyl ethyl ketone) in a selectivity of 70% of theory (cf. Example 1A). From this, the novel process can be used to obtain 3,3-dimethoxy-2-butanone in yields above 90% (cf. Example 1B), which can be converted into diacetyl by alkaline or, preferably, acidic hydrolysis in a manner known per se in virtually quantitative yield. This is therefore a very advantageous overall process for the preparation of diacetyl from the readily available methyl ethyl ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06316676B1 |
|---|
| Source dataset | uspto-grants-2001_11 |
|---|
| ORD ID | ord-c8deab39489a407b863091af1dbef2a3 |
|---|
| Source note | uspto-grants-2001_11 |
|---|