HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791036Generated: November 4, 2026
Methanesulfonamide → HCID 12010474, compound
https://huagongshe.com/reaction/1791036
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | HCID 11194472 | HCID 11194472 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | 2-Methylpropan-2-ol--water (1/1) | HCID 71401949 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Product | HCID 12010474 | HCID 12010474 | 95% |
Reaction Steps
160 mg (1 mmol) of 3-methylene-2,3-dihydro-1-benzoxepin, prepared according to example 23, are added to a mixture of 250 mg (1 mmol) of osmium tetroxide and 95 mg (1 mmol) of methanesulfonamide dissolved in 10 ml of a 1/1 water/tert-butanol mixture. After 12 hours at ambient temperature, 1.5 g of sodium bisulfite are introduced and the medium is stirred for one hour. Extraction with dichloromethane and then purification (purification is carried out by chromatography on silica gel (dichloromethane/methanol: 95/5)) provides 192 mg (95%) of 3-(hydroxymethyl)-2,3-dihydro-1-benzoxepin-3-ol in the form of a white solid; 1H NMR (300 MHz, CDCl3): 7.28–7.18 (m, 2H), 7.08–6.9 (m, 2H), 6.41 (d, J=12 Hz, 1H), 5.85 (d, J=11.2 Hz, 1H), 4.14 (d, J=11.7 Hz, 1H), 4.14 (d, J=11.7 Hz, 1H), 3.72–3.62 (m, 2H), 2.69 (broad s, 1H, OH), 2.28 (broad s, 1H, OH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071340B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-927e297db59546fc924cca8ee753e324 |
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| Source note | uspto-grants-2006_07 |
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