HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428023Generated: October 31, 2026
o-Fluorobenzaldehyde → 2-(Diethoxymethyl)-alpha-(2-fluorophenyl)-benzenemethanol
https://huagongshe.com/reaction/428023
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Reactant | 1-Bromo-2-(diethoxymethyl)benzene | HCID 3482778 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-(Diethoxymethyl)-alpha-(2-fluorophenyl)-benzenemethanol | HCID 18357546 | — |
Reaction Steps
A solution of 345 g of 2-bromobenzaldehyde diethyl acetal in 3 l of dry tetrahydofuran was cooled to −40° C. In one portion, 913 ml of a 1.6 M solution of butyllithium in hexane were added under vigorous stirring. The resulting solution was stirred for 0.5 h at −25° C., after which a solution of 140 ml of 2-fluorobenzaldehyde in 350 ml tetrahydrofuran was added drop-wise. In a period of 4 h, the mixture was allowed to reach room temperature. The resulting mixture was pored upon ice-water and extracted several times with ethyl acetate. The organic layers were combined, washed with water, dried over magnesium sulphate and evaporated to dryness under reduced pressure to yield 404 g of 2-(diethoxymethyl)-α-(2-fluorophenyl)-benzenemethanol as an oil, M.S. (C.I.) (M/Z): 305 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06313139B1 |
|---|
| Source dataset | uspto-grants-2001_11 |
|---|
| ORD ID | ord-0edb1aa8f4e248b5a0c1eab0eca70571 |
|---|
| Source note | uspto-grants-2001_11 |
|---|