HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870047Generated: October 30, 2026
3-Chlorobenzaldehyde → (4-Bromo-2,5-dichloro-3-thienyl)(3-chlorophenyl)methanol
https://huagongshe.com/reaction/870047
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Chlorobenzaldehyde | HCID 11477 | — |
| Reactant | 3,4-Dibromo-2,5-dichlorothiophene | HCID 7015318 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Bromo-2,5-dichloro-3-thienyl)(3-chlorophenyl)methanol | HCID 57900988 | — |
Reaction Steps
To a solution of 3,4-dibromo-2,5-dichlorothiophene (2.00 g, 6.43 mmol) in THF (18 mL) at −78° C., was added n-BuLi (2.5M in hexane, 2.57 mL, 6.43 mmol) dropwise. After 30 min., 3-chlorobenzaldehyde (0.732 mL, 6.43 mmol) was added dropwise to the yellow solution. The resulting solution was stirred at −78° C. for 30 min. and allowed to warm to 0° C. After 30 min., the reaction was quenched by the addition of 25% aq. NH4OAc. The aqueous layer was extracted with EtOAc and the combined organics were washed with water and brine, dried (Na2SO4) and concentrated. The crude product was purified by chromatography on silica gel (50:50 to 80:20 CHCl3/hexane) to afford the desired product as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969394B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-5ec3e8f4ff7345f4b17b6326447c023e |
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| Source note | uspto-grants-2015_03 |
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