HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Cyanomethyl 2-(allyloxy)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | 2-(Prop-2-en-1-yloxy)acetic acid | HCID 10997006 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Cyanomethyl 2-(allyloxy)acetate | HCID 91618380 | 60% |
Reaction Steps
2-(Allyloxy)acetic acid (0.500 g, 4.31 mmol) was dissolved in dichloromethane (20 ml), and 2-bromoacetonitrile (2.06 g, 17.18 mmol) and triethylamine (0.87 g, 8.61 mmol) were slowly added at room temperature. After stirring at room temperature for 3 hours, the reaction solution was concentrated under reduced pressure, and the resulting residue was purified by column chromatography (petroleum ether:ethyl acetate=20:1) to afford cyanomethyl 2-(allyloxy)acetate (0.40 g, 60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409952B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-15b1999e72884665812c6f34cdce6047 |
| Source note | uspto-grants-2016_08 |