HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 54478558, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 21286951 | HCID 21286951 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Product | HCID 54478558 | HCID 54478558 | 79% |
Reaction Steps
An ethyl ether solution of 13.8 g (0.05 moles) of 2,3-dihydro-2,3,5-trimethyl-6-(2-methyl-2-bromo-1-oxoethyl)-4H-pyran-4-one was dripped to ethylmagnesium bromide prepared from 1.5 g of magnesium and 6.6 g of ethyl bromide in 200 ml of ethyl ether. After the ether solution was agitated at room temperature for 1 hour, 1.2 g (0.05 moles) of magnesium were added and the mixture was agitated for 3 more hours. The reaction mixture was poured into 100 ml of dilute hydrochloric acid to concentrate the ether layer, thereby providing 7.9 g of 2,3-dihydro-2,3,5-trimethyl-6-(1-methyl-1-butenyl)-4H-pyran-4-one. The yield was 79%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04782168 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-9f31d433adcf4439b3b823881ce7df17 |
| Source note | uspto-grants-1988_11 |