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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036767Generated: November 1, 2026

Phthalimide → (S)-(+)-N-(2,3-Epoxypropyl)phthalimide

https://huagongshe.com/reaction/2036767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(-)-GlycidolHCID 6973630—
SolventTetrahydrofuranHCID 8028—
Product(S)-(+)-N-(2,3-Epoxypropyl)phthalimideHCID 71941273.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold solution of (S)-1-oxiranylmethanol (5 g, 67.5 mmol) and phthalimide (9.9 g, 67.3 mmol) in tetrahydrofuran (200 mL) in ice bath was added triphenylphosphine (17.9 g, 68.2 mmol) and diethyl azodicarboxylate (12.3 g, 70.6 mmol). The mixture was stirred at 0° C. for 2 h and at ambient temperature for 48 h. The mixture was concentrated under vacuum, and the oily residue was purified by flash silica column chromatography, yielding the desired product (10.1 g) as pale yellow solid: Rf=0.51 in 1:1 EtOAc/hexane. 1H-NMR (CDCl3, 300 MHz): δ (ppm) 7.76-7.64 (m, 2H), 7.63-7.60 (m, 2H), 3.9-3.8 (dd, 1H), 3.70-3.65 (dd, 1H), 3.15 (m, 1H), 2.70-2.67 (dd, 1H), 2.58-2.55 (dd, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575192B2
Source datasetuspto-grants-2013_11
ORD IDord-295d2435bdbb4388a8aea83951a1d19b
Source noteuspto-grants-2013_11