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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602130Generated: October 25, 2026

Phthalimide → tert-Butyl 2-((1,3-dioxoisoindolin-2-yl)methyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/602130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantTriphenylphosphineHCID 11776—
Reactanttert-Butyl 2-(hydroxymethyl)morpholine-4-carboxylateHCID 5201202—
ReactantDiethylazodicarboxylate tolueneHCID 66777355—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 2-((1,3-dioxoisoindolin-2-yl)methyl)morpholine-4-carboxylateHCID 5899266097%

Reaction Steps

Triphenylphosphine (506 mg, 1.87 mmol) and phthalimide (275 mg, 1.87 mmol) were added to 4-(tert-butoxycarbonyl)morpholin-2-yl methanol (340 mg, 1.56 mmol) in tetrahydrofuran (3 mL). The mixture was stirred at room temperature for 5 min, followed by addition of a 40% diethyl azodicarboxylate/toluene solution (1.06 mL, 2.34 mmol) and stirring at room temperature for 4 hours. Subsequently, ethyl acetate was added and the mixture washed sequentially with tap water and brine. The mixture was then dried over magnesium sulfate and the solvent was evaporated. Purification of the residue by silica gel column chromatography (hexane:ethyl acetate=10:1->3:1) gave 524 mg (97%) of the desired compound as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902367B2
Source datasetuspto-grants-2011_03
ORD IDord-68037ced14ef487da4480e0c343604ce
Source noteuspto-grants-2011_03