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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848966Generated: October 30, 2026

4-Hydroxybenzaldehyde → HCID 22593913, compound

https://huagongshe.com/reaction/848966

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant4H-1,4-Benzothiazine-4-ethanol, 2,3-dihydro-HCID 11469633—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22593913HCID 2259391344%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a mixture of 4-hydroxy benzaldehyde (1.8 g, 14.8 mmol) and triphenyl phosphine (4.85 g, 18.5 mmol) in tetrahydrofuran (15 ml) was added 2-(2,3-dihydro-1,4-benzothiazin-4-yl)ethanol (2.39 g, 12.3 mmol) and diisopropyl azodicarboxylate (3.74 g, 18.5 mmol) in THF (20 ml) at 25° C. The reaction mixture was stirred for 12 h at 25° C. Water (100 ml) was added and the mixture was extracted with ethyl acetate (2×100 ml). The organic extracts were dried (Na2SO4) and solvent was evaporated under reduced pressure. The crude product was chromatographed over silica gel using a mixture of methanol and chloroform (5:95) as an eluent to afford the title compound (1.6 g, 44%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06011031
Source datasetuspto-grants-2000_01
ORD IDord-0cdaa2cd1b5a4decbb7c5c7504ba344e
Source noteuspto-grants-2000_01