HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611398Generated: November 1, 2026
Ammonium Chloride → HCID 19600213, compound
https://huagongshe.com/reaction/611398
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 19599952 | HCID 19599952 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | HCID 178418255 | HCID 178418255 | — |
| Product | HCID 19600213 | HCID 19600213 | — |
Reaction Steps
To a solution of 0.142 g (0.487 mmol) of 4-(5,7-dihydro-4H-furo[2,3-c]pyridin-6-ylsulfonyl)benzaldehyde in 30 ml of tetrahydrofuran, phenylmagnesium bromide in tetrahydrofuran (prepared from 2.0 g of bromobenzene and 0.31 g of magnesium in 30 ml of tetrahydrofuran) was added at room temperature until the starting material disappeared on thin-layer chromatography (TLC). To the reaction mixture, aqueous ammonium chloride was added, followed by stirring and 3 extractions with ethyl acetate. The combined organic layer was dried over anhydrous magnesium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (hexane/ethyl acetate=3/1 to 2/1) to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998433 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-4fb9e0a12338499997ac3c8ef051b736 |
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| Source note | uspto-grants-1999_12 |
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