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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664126Generated: November 1, 2026

Triphenylphosphine → HCID 16753952, compound

https://huagongshe.com/reaction/1664126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 16753951HCID 16753951—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 16753952HCID 1675395235%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-azidomethyl-5-fluoro-N,N-dimethyl-benzenesulfonamide (660 mg, 2.6 mmol) in tetrahydrofuran (10 mL) and water (2 mL) was added triphenylphosphine (740 mg, 2.8 mmol), and the mixture stirred under nitrogen for 1 hr. The tetrahydrofuran was evaporated in vacuo and a mixture of the residue and 6N HCl (3 mL) in MeOH (5 mL) was heated at 80° C. for 20 hrs. This was washed with CH2Cl2, and the aqueous phase made basic with dilute NH4OH then extracted with CH2Cl2. The organic extract was dried (Na2SO4), filtered and concentrated to provide 210 mg (0.91 mmol, Yield 35%) of the title compound; 1H NMR (500 MHz, CDCl3) δ ppm: 2.84 (6H, s) 4.10 (2H, s) 7.23-7.29 (1H, m) 7.53-7.60 (2H, m); LC/MS m/z 233 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039458B2
Source datasetuspto-grants-2011_10
ORD IDord-e6603ca86cec4b338a981b8c4252d1be
Source noteuspto-grants-2011_10