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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | tert-Butyl [2-phthalimido-1-(methylsulfanylmethyl)ethyl]carbamate | HCID 24720892 | — |
| Product | tert-butyl [1-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-3-(methylsulfonyl)propan-2-yl]carbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216173B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-b2f6f1edc8c0486bb8ce41aa884cc6e9 |
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| Source note | uspto-grants-2015_12 |
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