HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176717Generated: November 2, 2026
Triphenylphosphine → HCID 11539237, compound
https://huagongshe.com/reaction/1176717
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-ethyl-4-nitrobenzenesulfonamide | HCID 232621 | — |
| Reactant | HCID 15647030 | HCID 15647030 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11539237 | HCID 11539237 | 50.4% |
Reaction Steps
Methylene chloride (60 mL), cis-4-hydroxy-5,6-dihydro-6-methyl-4-H-thieno-[2,3-b]-thiopyran-7,7-dioxide (5 g), N-ethyl-4-nitrobenzene-sulfonamide (6.86 g) and triphenyl-phosphine (8.42 g) are mixed under nitrogen atmosphere. The mixture is cooled to under −20° C. and diisopropyl azadicarboxylate (5.9 mL) is added, maintaining the temperature under −20° C. The temperature is allowed to rise to 20-25° C. The obtained mixture is treated with 5% NaOH (125 mL) and the resulting organic phase is vacuum distilled to dryness. The residue is chromatographed in a column (ethyl acetate/heptane, 2/1), obtaining 4.97 g of trans-4-[N-ethyl-N-(4-nitrobenzenesulfonyl)amino]-5,6-dihydro-6-methyl-4-H-thieno-[2,3-b]-thiopyran-7,7-dioxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842821B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-4d200f30753241b8a8b2e083ffe991e8 |
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| Source note | uspto-grants-2010_11 |
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