HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → 1-(3-Butynyl)-3,6-dimethoxy-2,4,5-trimethylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1-(Chloromethyl)-2,5-dimethoxy-3,4,6-trimethylbenzene | HCID 10878929 | — |
| Catalyst | Sodium Iodide | HCID 5238 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3-Butynyl)-3,6-dimethoxy-2,4,5-trimethylbenzene | HCID 21608417 | 96.3% |
Reaction Steps
A solution of chloromethyltrimethylhydroquinone dimethyl ether (7.5 g; 32 mmol) in THF (20 ml) was treated dropwise at 0° with a freshly Prepared solution of a Grignard reagent Prepared from 1.9 g of magnesium shavings and 4.91 ml (65 mmol) of propargyl bromide. After the addition of solid sodium iodide (0.42 g) the mixture was warmed to room temperature and stirred overnight. Thereafter, the reaction mixture was diluted with ether and washed with 2N hydrochloric acid. The ethereal solution was deacidified with bicarbonate, dried and freed from solvent. Distillation (0.04 mbar; 140° C.) of the residue gave 7.16 g of 1-(3-butynyl)-3,6-dimethoxy-2,4,5-trimethylbenzene; melting point: 54° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05110955 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-a79de7c350f041f6a90a4184f9a6ada7 |
| Source note | uspto-grants-1992_05 |