HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209568Generated: October 31, 2026
hydroxylamine-O-sulfonic acid → HCID 15010183, compound
https://huagongshe.com/reaction/2209568
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | hydroxylamine-O-sulfonic acid | HCID 76284 | — |
| Reactant | 3-(4-Chlorophenyl)-1H-pyrrole-2-carboxaldehyde | HCID 15753017 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15010183 | HCID 15010183 | 63.7% |
Reaction Steps
A mixture of 0.63 g (3.1 mmol) of 3-(p-chlorophenyl)-pyrrole-2-carboxaldehyde in 10 mL of water is stirred and ice-cooled while 0.52 g (4.6 mmol) of hydroxylamine-O-sulfonic acid in 10 mL of water is slowly added. After the addition, the cooling bath is removed and the mixture is heated for 25 minutes. On cooling, the resulting solid is collected and shown, by NMR, to be a mixture of product and starting aldehyde. This mixture is reacted in the same manner with an additional 0.49 g (4.2 mmol) of hydroxylamine-O-sulfonic acid in a total of 30 mL of water. The mixture is heated at 60°-70° C. for 2 hours. The mixture is cooled and the resulting solids are collected and purified by chromatography or silica gel using 1:1 ethyl acetate hexane to give 0.40 g of pink solid, m.p. 114°-115° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05455263 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-d5a774f21383473b84d8b8daa2e939f9 |
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| Source note | uspto-grants-1995_10 |
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