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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766827Generated: November 1, 2026

N-Hydroxyphthalimide → [3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yloxy)-2,2-dimethyl-propyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1766827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxyphthalimideHCID 10665—
ReactantTriphenylphosphineHCID 11776—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactanttert-butyl N-(3-hydroxy-2,2-dimethylpropyl)carbamateHCID 21263232—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yloxy)-2,2-dimethyl-propyl]-carbamic acid tert-butyl esterHCID 6886249111.4%

Reaction Steps

Diethylazodicarboxylate (8.26 mL, 52.4 mmol) was added to a solution of (3-hydroxy-2,2-dimethyl-propyl)-carbamic acid tert-butyl ester (10.2 g, 49.9 mmol), N-hydroxyphthalimide (8.15 g, 49.9 mmol) and triphenylphosphine (13.1 g, 49.9 mmol) in THF (200 mL). The solution was stirred at room temperature for 16 hours after which time it was diluted with dichloromethane and passed through a plug of silica gel, eluting with dichloromethane. The product containing fractions were concentrated to a yellow liquid, which was further purified by flash column chromatography (dichloromethane to 4:1 dichloromethane/ethyl acetate) to provide pure desired product (1.98 g, 11%) as a waxy white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230099B2
Source datasetuspto-grants-2007_06
ORD IDord-d72a0673189944ffbceb022c0de16bf4
Source noteuspto-grants-2007_06