HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → 2-[(6-Bromohexanoyl)oxy]propyl acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 6-Bromohexanoic acid | HCID 20210 | — |
| Reactant | 2-Hydroxypropyl acrylate | HCID 61249 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[(6-Bromohexanoyl)oxy]propyl acrylate | HCID 59005029 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a 0° C. cooled mixture of 6-bromohexanoic acid (9.89 g), 2-hydroxypropyl acrylate (6 g), in CH2Cl2 (30 ml), EDC (7.89 g) was added. After being stirred for 30 min the reaction mixture was diluted with additional 20 ml of CH2Cl2 and stirring was continued for 16 h at room temperature. It was then filtered over celite and the filtrate was evaporated to dryness. The obtained beige-yellow residue was purified by silica column chromatography to give nearly pure material as transparent oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08105662B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-0e5407f232de4411a3a215497f6e7f7d |
| Source note | uspto-grants-2012_01 |