HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Methylbut-2-en-1-yl bromoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Methyl-2-buten-1-OL | HCID 11173 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Methylbut-2-en-1-yl bromoacetate | HCID 15141476 | 64.2% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A 1-liter flask was charged with 43.9 g (0.51 mol) of 3-methyl-2-buten-1-ol, 51.6 g (0.51 mol) of triethylamine and 300 ml of dichloromethane, and the mixture was cooled down to 0° C. While stirring the mixture at 0° C., 100.9 g (0.50 mol) of bromoacetyl bromide were added dropwise over 1 hour, followed by stirring further for 3 hours at room temperature. Solids were separated by filtration from the resultant reaction mixture, and the filtrate was washed 3 times with water and distilled to obtain 66.5 g of 3-methyl-2-butenyl bromoacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06010826 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-5ca740f336de49a8a42daa882b945945 |
| Source note | uspto-grants-2000_01 |