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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504832Generated: October 30, 2026

Methanol → tert-butyl [1-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-3-(methylsulfonyl)propan-2-yl]carbamate

https://huagongshe.com/reaction/1504832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactanttert-Butyl [2-phthalimido-1-(methylsulfanylmethyl)ethyl]carbamateHCID 24720892—
Producttert-butyl [1-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-3-(methylsulfonyl)propan-2-yl]carbamateHCID 76781197—

Reaction Steps

To a solution of tert-butyl [1-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-3-(methylsulfanyl)propan-2-yl]carbamate (10.0 g, 28.6 mmol) in methanol (100 mL) was added Oxone (53.1 g, 85.7 mmol) and water (100 mL). The reaction mixture was stirred at ambient temperature for 3 hours and then quenched with 20% aqueous sodium bisulfite solution, diluted with water, and extracted with DCM. The combined organic layers were washed with brine, dried over sodium sulfate, filtered, and concentrated under reduced pressure to give tert-butyl [1-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-3-(methylsulfonyl)propan-2-yl]carbamate which was used without further purification. MS ESI calc'd. for C17H22N2O6SNa [M+H]+ 405. found 405. 1H NMR (400 MHz, CD3OD) δ 7.89-7.81 (m, 4H), 4.51-4.48 (m, 1H), 3.88-3.82 (m, 2H), 3.44-3.40 (m, 2H), 3.01 (s, 3H), 1.26 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216173B2
Source datasetuspto-grants-2015_12
ORD IDord-b2f6f1edc8c0486bb8ce41aa884cc6e9
Source noteuspto-grants-2015_12