HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909774Generated: October 26, 2026
Ammonium Chloride → 5-Bromo-2-chlorobenzaldehyde
https://huagongshe.com/reaction/909774
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 5-Bromo-2-chloro-N-methoxy-N-methylbenzamide | HCID 53418379 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Bromo-2-chlorobenzaldehyde | HCID 10608925 | 95.1% |
Reaction Steps
LiAlH4 (1.47 g, 0.0388 mol) was added little by little to a tetrahydrofuran (108 mL) solution of 5-bromo-2-chloro-N-methoxy-N-methylbenzamide (10.8 g, 0.0388 mol) so that the internal temperature did not exceed −10° C. The reaction mixture was stirred at −15° C. for one hour and carefully added with a saturated ammonium chloride aqueous solution and deposited insolubles were filtered off with celite. After the filtrate was extracted with ethyl acetate, the organic layer was washed with 1M hydrochloric acid, a saturated sodium bicarbonate aqueous solution, brine, and then dried with anhydrous magnesium sulfate. After the desiccant was filtered off, the solvent was evaporated under reduced pressure to obtain 5-bromo-2-chlorobenzaldehyde (8.1 g, 95%) as a pale yellow crystal. This was used in the next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017792B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-f658e5e1362c4965aaea6ab3bc4d48fd |
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| Source note | uspto-grants-2011_09 |
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