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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952434Generated: November 3, 2026

Triphenylphosphine → N-(4-phenylbenzenesulfonyl)aziridine

https://huagongshe.com/reaction/1952434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(+/-)-N-Boc-trans-3-(4-phenylbenzenesulfonamido)-4-hydroxypyrrolidineHCID 86654490—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-phenylbenzenesulfonyl)aziridineHCID 86654492145.5%

Reaction Steps

To a stirred solution of Ph3P (242 mg, 0.92 mmol) and (±)-N-Boc-trans-3-(4-phenylbenzenesulfonamido)-4-hydroxypyrrolidine (350 mg, 0.84 mmol) in THF (20 mL) at 0° C. was added diethyl azodicarboxylate (DEAD) (160 μL, 1.0 mmol) dropwise. The reaction mixture was stirred at room temperature overnight, then it was evaporated under reduced pressure. The residue was purified by flash chromatography (30% ethyl acetate in hexane) to give the N-(4-phenylbenzenesulfonyl)aziridine (317 mg, 95%): 1H NMR (300 MHz, CDCl3) δ 8.01 (d, J=8, 2H), 7.76 (d, J=8, 2H), 7.62 (d, J=7, 2H), 7.48 (m, 3H), 3.73 (dd, J=12, 2, 2H), 3.64 (dd, J=6, 2, 1H), 3.53 (dd, J=6, 2, 1H), 3.40 (m, 2H), 1.42 (s, 9H); HRMS (ESI) calculated for C21H24N2O4SNa+ 423.1355. found 423.1355.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404866B2
Source datasetuspto-grants-2013_03
ORD IDord-207c8a69cae74ff3b256128035116047
Source noteuspto-grants-2013_03