HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 12895736, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 2-Chloro-5-(chloromethyl)thiophene | HCID 583079 | — |
| Reactant | HCID 178455850 | HCID 178455850 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 12895736 | HCID 12895736 | 195.9% |
Reaction Steps
A solution of allyl magnesium bromide (from 14.6 g of magnesium and 24.2 g (0.2 M) of allyl bromide) in 100 ml ether is added dropwise with stirring to 29.9 g of 5-chloro-2-chloromethylthiophene in 10 ml ether over half an hour and the resulting mixture heated under reflux overnight. The mixture is then poured into 300 ml ice cold dilute sulfuric acid, the ether layer separated and the aqueous phase extracted with 200 ml of ether. The combined ethereal solutions are washed with aqueous potassium carbonate, dried over MgSO4 and evaporated to give crude 4-(5-chloro-2-thienyl)-1-butene as a yellow oil (34 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04272545 |
| Source dataset | uspto-grants-1981_06 |
| ORD ID | ord-11bf73e510b5456ba3a8bad29c96dd32 |
| Source note | uspto-grants-1981_06 |