HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 86737907, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | MAGNESIUM SILICATE (synthetic) | HCID 61680 | — |
| Reactant | 1-(Bromomethyl)-3-phenoxybenzene | HCID 94544 | — |
| Reactant | HCID 53962544 | HCID 53962544 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86737907 | HCID 86737907 | 46.9% |
Reaction Steps
A solution of 3.7 g of 3-phenoxybenzyl bromide and 2.8 g of (1R,cis)-2,2-dimethyl-3-((allyloxyimino)methyl)cyclopropanecarboxylic acid (prepared by a method similar to that shown in Embodiment I) and 1.4 g of triethylamine in 30 ml of ethyl acetate was refluxed for 21/2 hours. The reaction mixture was diluted with ether and washed with water. The ether phase was dried over magnesium sulfate, filtered and stripped to give an oil. This oil in methylene chloride was passed through a florisil column to give 2.5 g of the desired product as an oil [α]D25 +22.9° (CHCl; c=0.012 g/cc).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04282249 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-2f4754bf36a74072aaad5c8fee0a1a33 |
| Source note | uspto-grants-1981_08 |