HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987048Generated: October 30, 2026
4-Nitrobenzaldehyde → HCID 6610568, compound
https://huagongshe.com/reaction/987048
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Cysteine Hydrochloride | HCID 60960 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 6610568 | HCID 6610568 | 87% |
Reaction Steps
3 g (17.08 mmoles) of L-Cysteine hydrochloride and 2.18 g (22.2 mmoles) of sodium acetate are dissolved in 75 ml of water. The solution is agitated vigorously during the addition by portions, of 3.10 g (20.5 mmoles) of 4-nitrobenzaldehyde in solution in 80 ml of 95% ethanol. A white precipitate rapidly appears in this pale yellow solution which forms abundantly. Agitation is maintained for one hour, the reaction mixture is then cooled down to 0° C. and filtered. The precipitate is successively rinsed with 200 ml of water, 100 ml of cold ethanol and 100 ml of ethyl ether. After drying, a white powder is obtained with a yield of 87%. Melting point: 120-121° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06630461B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-c9428b8a8a9b442286641404088bcad1 |
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| Source note | uspto-grants-2003_10 |
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