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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176717Generated: November 2, 2026

Triphenylphosphine → HCID 11539237, compound

https://huagongshe.com/reaction/1176717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium HydroxideHCID 14798—
ReactantN-ethyl-4-nitrobenzenesulfonamideHCID 232621—
ReactantHCID 15647030HCID 15647030—
SolventDichloromethaneHCID 6344—
ProductHCID 11539237HCID 1153923750.4%

Reaction Conditions

Temperature-20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842821B2
Source datasetuspto-grants-2010_11
ORD IDord-4d200f30753241b8a8b2e083ffe991e8
Source noteuspto-grants-2010_11