HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676516Generated: October 27, 2026
Boron trifluoride etherate → HCID 58015015, compound
https://huagongshe.com/reaction/1676516
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | N-(benzotriazol-1-ylmethyl)cyclopentanamine | HCID 5235843 | — |
| Reactant | (2,2-Dichloro-1-methoxy-vinyloxy)-trimethylsilane | HCID 11435856 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58015015 | HCID 58015015 | 50% |
Reaction Steps
To a solution of 4.3 g (0.02 mole) of benzotriazol-1-ylmethyl-cyclopentyl-amine and 6.4 g (0.030 mole) of (2,2-dichloro-1-methoxy-vinyloxy)-trimethyl-silane in 140 ml of anhydrous dichloromethane was added dropwise 3.7 ml (0.030 mole) of boron trifluride diethyl etherate at 0 degrees. The reaction was stirred at 0 degrees for 1 hour and then at room temperature for 24 hours. The reaction was quenched by the addition of 10% aqueous sodium carbonate and extracted with dichloromethane. The organic layer was washed with saturated sodium carbonate, brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. Purification by silica gel chromatography, eluting with hexane-ethyl acetate (gradient, 100:0-85:15) gave 2.4 g of 2,2-dichloro-3-cyclopentylamino-propionic acid methyl ester as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08003785B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-e20c866e1bea4a4ea87b82551f32de27 |
|---|
| Source note | uspto-grants-2011_08 |
|---|