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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387186Generated: October 31, 2026

Triphenylphosphine → HCID 59372566, compound

https://huagongshe.com/reaction/2387186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 57515616HCID 57515616—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59372566HCID 59372566—

Reaction Steps

Crude tert-butyl N-(3-nitrobenzylsulfamoyl)carbamate, triphenylphosphine (2 g) and diisopropyl azadicarboxylate (DIAD, 1.6 g) were dissolved in THF (20 mL) and ethanol (0.47 mL). The solution was stirred at ambient temperature overnight. The reaction solution was evaporated to dryness. The residue was dissolved in methanol (10 mL) and treated with 4.0 M HCl in dioxane (10 mL). It was stirred at rt overnight and then evaporated. The residue was diluted with ethyl acetate (100 mL) and washed with NaHCO3 aq. (2×100 mL). The organic solution was evaporated and purified by flash column chromatography (EtOAc/hexane=1/2, 1/1) to give N-(3-nitrobenzyl)-N′-ethylsulfamide. 1H NMR (DMSO-d6): δ 1.02 (t, J=7.2 Hz, 3H), 2.82 (p, J=6.9 Hz, 2H), 4.14 (d, J=6.6 Hz, 2H), 6.93 (t, J=5.4 Hz, 1H), 7.54 (t, J=6.3 Hz, 1H), 7.61 (t, J=7.8 Hz, 1H), 7.77 (d, J=7.2 Hz, 1H), 8.10 (d, J=8.1 Hz, 1H), 8.20 (s, 1H); LCMS: purity: 1.2 g, 88.4%; MS (m/e): 260.16 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268851B2
Source datasetuspto-grants-2012_09
ORD IDord-719ec82f0f854f09ac544068b8d34677
Source noteuspto-grants-2012_09