HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727249Generated: October 29, 2026
3,4-Dichlorobenzaldehyde → HCID 22101839, compound
https://huagongshe.com/reaction/727249
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dichlorobenzaldehyde | HCID 22710 | — |
| Reactant | 2-Bromothiazole | HCID 76430 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 22101839 | HCID 22101839 | — |
Reaction Steps
2-Bromothiazole (5 g) in dry diethyl ether (20 ml) was added dropwise to a stirred solution of n-butyllithium (1.6M in hexanes, 21 ml) in diethyl ether (20 ml) at -70° C. under an atmosphere of dry nitrogen. After 30 minutes, trimethylsilylchlorlde (3.9 ml) was added and the mixture was allowed to warm to 0° C. The mixture was then cooled to -70° C. and further n-butyllithium (21 ml) was added. The mixture was warmed to 0° C. and after 30 minutes was cooled again to -70° C. and 3,4-dichlorobenzaldehyde (5.8 g) in diethyl ether (40 ml) was added. The mixture was then allowed to warm to room temperature and after 30 minutes saturated aqueous sodium hydrogen carbonate was added. The mixture was extracted with dichloromethane and the material thus obtained was purified by chromatography on silica gel to give the title compound. The hydrochloride salt was prepared. M.p. 167°-170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05712299 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-d59c97b7719a48c5ae33033070e6000f |
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| Source note | uspto-grants-1998_01 |
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