HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503176Generated: October 29, 2026
2-Naphthalenecarboxaldehyde → HCID 22260898, compound
https://huagongshe.com/reaction/503176
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Naphthalenecarboxaldehyde | HCID 6201 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 2-Bromo-5-fluoroanisole | HCID 7018043 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 22260898 | HCID 22260898 | 82.7% |
Reaction Steps
In an atmosphere of nitrogen gas, 2.38 ml of a 2.66 M solution of n-butyllithium in hexane was added to a solution of 0.64 g of N,N-diisopropylamine in 9 ml tetrahydrofuran at −78° C. After stirring at the same temperature for 1 hour, 1.18 g of 1-bromo-4-fluoro-2-methoxy-benzene obtained in Production Example II-1-a was added dropwise. After stirring at the same temperature for 1 hour and 20 minutes, a solution of 0.99 g of 2-naphthoaldehyde in 4 ml tetrahydrofuran was added dropwise. After stirring at the same temperature for 1 hour and 20 minutes, water was added under ice-cooling and the mixture was extracted with diethyl ether for two times. The extract was sequentially washing with water and brine, dried over anhydrous magnesium sulfate and the solvent was evaporated. The crude product was purified and separated by silica gel column chromatography, to give 1.72 g of the title compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07776890B2 |
|---|
| Source dataset | uspto-grants-2010_08 |
|---|
| ORD ID | ord-02beba5b28e8428f909bf259bd47305d |
|---|
| Source note | uspto-grants-2010_08 |
|---|