HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169965Generated: October 28, 2026
2,3-Difluorobenzaldehyde → HCID 66776591, compound
https://huagongshe.com/reaction/1169965
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Difluorobenzaldehyde | HCID 137664 | — |
| Reactant | 1-(diethoxymethyl)-1H-imidazole | HCID 3849535 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66776591 | HCID 66776591 | 64.6% |
Reaction Steps
To a solution of 1-(diethoxymethyl)-1H-imidazole (1.65 ml, 10.1 mmol) in tetrahydrofuran (15 ml), at −60° C. and under nitrogen, was added n-butyllithium (2.5 M in hexanes, 4.03 ml, 10.1 mmol). The reaction mixture was stirred at −60° C. for 1 h, before addition of 2,3-difluorobenzaldehyde (1.00 ml, 9.2 mmol), and then allowed to warm to room temperature over 18 h. The mixture was concentrated in vacuo and to the residue was added ethyl acetate (50 ml) and hydrochloric acid (3M, 50 ml). The two layers were separated and the aqueous phase was basified with aqueous sodium hydroxide solution (20%) and extracted with ethyl acetate (3×100 ml). The combined organic phases were dried (MgSO4) and concentrated in vacuo and the residue was re-crystallised from 2-propanol to give the title compound (1.25 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07825149B2 |
|---|
| Source dataset | uspto-grants-2010_11 |
|---|
| ORD ID | ord-ba9b3117e56349ed82981baf22799b49 |
|---|
| Source note | uspto-grants-2010_11 |
|---|