HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871133Generated: October 31, 2026
3-Bromo-2-fluorobenzaldehyde → HCID 71743203, compound
https://huagongshe.com/reaction/871133
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromo-2-fluorobenzaldehyde | HCID 22019361 | — |
| Reactant | HCID 178418630 | HCID 178418630 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 71743203 | HCID 71743203 | 100% |
Reaction Steps
To a solution of 3-bromo-2-fluorobenzaldehyde (0.500 g, 2.463 mmol) in THF (10.71 mL) cooled to −78° C. was added cyclopropylmagnesium bromide (5.91 mL, 2.96 mmol). The reaction mixture was maintained at −78° C. for at least 2 hr, then allowed to warm to room temperature. During this time, additional cyclopropylmagnesium bromide (5.91 mL, 2.96 mmol) was added. After 30 min, the reaction was quenched with a saturated aqueous solution of NH4Cl. The reaction mixture was diluted with CH2Cl2. The layers were separated and the aqueous phase extracted with CH2Cl2 (2×). The organics were combined, dried over Na2SO4, filtered, and concentrated to afford the title compound (0.604 g, 2.464 mmol, 100% yield) as a yellow residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08969586B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-bfcce3529880483d9347f18ca0a54bc0 |
|---|
| Source note | uspto-grants-2015_03 |
|---|