HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413578Generated: October 30, 2026
Benzenesulfinic acid → (2RS,7S)-2-(benzenesulfonyl)-7-(4-fluorophenoxymethyl)oxepane
https://huagongshe.com/reaction/413578
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfinic acid | HCID 12057 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | (6S)-7-(4-fluorophenoxy)-6-hydroxyheptanal | HCID 59064024 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2RS,7S)-2-(benzenesulfonyl)-7-(4-fluorophenoxymethyl)oxepane | HCID 70026601 | 81% |
Reaction Steps
25% HCl was added dropwise to sodium salt of benzenesulfinic acid (5 g, 30.5 mmol) until the solid dissolved. The reaction mixture was extracted with EtOAc, dried over Na2SO4 and concentrated to give benzenesulfinic acid (3.9 g, 90%). To an ice-cold mixture of benzene sulfinic acid (1.8 g, 12.4 mmol) and CaCl2, (1.4 g, 12.5 mmol) in dry methylene chloride (50 ml) was added dropwise a solution of (6S)-7-(4-fluorophenoxy)-6-hydroxy-heptanal (2 g, 8.3 mmol) in methylene chloride (10 ml). The reaction mixture was stirred for 3 hours and filtered through celite, and washed with methylene chloride. The combined organic layer was washed with saturated aqueous Na2CO3, water, brine and dried over Na2SO4. Solvent was removed under reduced pressure and the residue was purified by silica gel chromatography using EtOAC-hexane (1:6) as eluent to give (2RS,7S)-2-(benzenesulfonyl)-7-(4-fluorophenoxymethyl)oxepane (2.45 g, 80.8%); 1H-NMR (CDCl3, 200 Hz): δ 1.39-2.20 (m, 7H), 2.5 (m, 1H), 3.57-3.90 (m, 2H), 4.45 (m, 1H), 4.72 (dd, J=6.6, 12.0 Hz, 1H), 6.57-7.00 (m, 4H), 7.36-7.96 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06566538B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-3d08109c29d64ee6ac11cb4047d2d47c |
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| Source note | uspto-grants-2003_05 |
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