HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19787Generated: October 27, 2026
Water → 3-(4-Tert-butylbenzyl)-[1,2,3]oxathiazolidine 2,2-dioxide
https://huagongshe.com/reaction/19787
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 3-(4-Tert-butylbenzyl)-[1,2,3]oxathiazolidine 2-oxide | HCID 68561052 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(4-Tert-butylbenzyl)-[1,2,3]oxathiazolidine 2,2-dioxide | HCID 86613991 | 76% |
Reaction Steps
To a solution of 2-(4-tert-butylbenzylamino)-ethanol (1190 mg, 5.74 mmol) and triethylamine (3200 μl, 22.96 mmol) in DCM (15 ml) at −15° C. was added a solution of thionylchloride (544 PI, 7.46 mmol) in DCM (4 ml) over 10 min. The reaction mixture was stirred at −10° C. for 30 min, filtered and the filtrate was concentrated in vacuo. The residue was purified by flash column chromatography to give the desired compound (790 mg, 54%) as a white solid. To a mixture of 3-(4-tert-butylbenzyl)-[1,2,3]oxathiazolidine 2-oxide (790 mg, 3.12 mmol) in DCM (20 ml), acetonitrile (8 ml) and water (8 ml), at 0° C. was added NaIO4 (867 mg, 4.05 mmol) followed by RuO2 (2 mg). The reaction mixture was stirred at 0° C. for 2 h. Water was added and the phases were separated and the aqueous phase was extract with ethyl acetate. The organic layers were combined washed with brine, dried (MgSO4), and concentrated in vacuo. The residue was then purified by flash column chromatography to give the desired product (640 mg, 76%) as an off white solid. MS (ISP) 287.0 (M+NH4)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745477B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-eaeeb894fa1241019c2eac0240bf2a0b |
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| Source note | uspto-grants-2010_06 |
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