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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484810Generated: October 30, 2026

N-Hydroxyphthalimide → HCID 14207366, compound

https://huagongshe.com/reaction/484810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxyphthalimideHCID 10665—
ReactantTriphenylphosphineHCID 11776—
Reactant3-Thietan-1-olHCID 82532—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14207366HCID 1420736638.5%

Reaction Conditions

Temperature40 °C

Reaction Steps

Diethyl azodicarboxylate (4.3 g) was added all at once to a stirred mixture of 3-thietanol (2.0 g), N-hydroxyphthalimide (3.6 g) and triphenylphosphine (5.8 g) in dry tetrahydrofuran (100 ml) at room temperature. The temperature of the reaction mixture was raised to 40° C. The mixture became clear solution and was stirred for 12 hours at room temperature. Tetrahydrofuran was evaporated in vacuo and the residue was dissolved in ethyl acetate (50 ml). The insoluble substance was filtered off. The filtrate was washed three times with a saturated aqueous solution of sodium bicarbonate (50 ml) and with a saturated aqueous solution of sodium chloride (50 ml), dried over magnesium sulfate and evaporated. The residue was dissolved in methylene chloride (50 ml), subjected to column chromatography on silica gel and eluted with methylene chloride. The fractions containing the object compound were collected and evaporated in vacuo to give N-(3-thietanyloxy)phthalimide (2.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04533738
Source datasetuspto-grants-1985_08
ORD IDord-7ff0fad4d88442ac98e7c94b52fe8158
Source noteuspto-grants-1985_08