HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 4H-1,3-Dioxin-4-one, 5-bromo-2,2,6-trimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2,2,6-Trimethyl-4H-1,3-dioxin-4-one | HCID 79368 | — |
| Reactant | Diethylether hexane | HCID 21584099 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4H-1,3-Dioxin-4-one, 5-bromo-2,2,6-trimethyl- | HCID 10353435 | 75% |
Reaction Steps
Bromine (0.105 mol, 5.38 ml) was added dropwise to a 20° C. solution of 2,2,6-trimethyl-4H-1,3-dioxin-4-one (TKD, 0.1 mol, 14.2 g) in 100 ml CH2Cl2 over five minutes. The reaction solution was rapidly decolorized and hydrogen bromide evolved. After 15 minutes, the solvent was removed in vacuo to provide 22 g (99%, >95% pure by NMR) of a pale yellow oil which solidified upon refrigeration. Flash chromatography (10% ether/hexane on silica) afforded 16.5 g (75%) of the title compound as colorless plates.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04582913 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-c39d5e366b2f440fac5b146d43dae0f8 |
| Source note | uspto-grants-1986_04 |