HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061916Generated: November 2, 2026
1-Benzothiophene-3-carbaldehyde → HCID 11999023, compound
https://huagongshe.com/reaction/2061916
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Benzothiophene-3-carbaldehyde | HCID 227328 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-Piperidinesulfonamide, 4-phenyl- | HCID 11999022 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 11999023 | HCID 11999023 | — |
Reaction Steps
4-Phenyl-piperidine-1-sulfonic acid amide (1.5 g, 6.24 mmol) was dissolved in ethanol (20 mL). Benzo[b]thiophene-3-carbaldehyde (1.0 g, 6.24 mmol) was then added and the reaction mixture was warmed to 45° C. overnight. The reaction mixture was cooled to room temperature and then treated with sodium borohydride (0.2 g, 5.29 mmol). The reaction was then quenched by addition of 1N HCl. The reaction mixture was stirred overnight. The product precipitated from solution and was removed by vacuum filtration to yield the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08283478B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-6e44a8b456864583bab24441660ce391 |
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| Source note | uspto-grants-2012_10 |
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