HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413568Generated: October 31, 2026
Benzenesulfinic acid → HCID 22959677, compound
https://huagongshe.com/reaction/413568
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfinic acid | HCID 12057 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | HCID 20588440 | HCID 20588440 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22959677 | HCID 22959677 | 76.7% |
Reaction Steps
25% HCl was added dropwise to benzenesulfinic acid sodium salt (0.6 g), until the solid dissolved. This mixture was extracted with ethyl acetate (15 ml) dried (Na2SO4) and concentrated to give benzenesulfinic acid (0.4 g). To an ice-cooled mixture of benzenesulfinic acid (0.32 g, 2.23 mmol) and calcium chloride (0.25 g, 2.23 mmol) in dry CH2Cl2 a solution of (2RS,6S)-6-(4-fluorophenoxymethyl)-2-hydroxy-tetrahydropyran (0.42 g, 1.86 mmol) in dry CH2Cl2 (5 ml) was added. The reaction mixture was stirred for 4 h, filtered through celite and washed with CH2Cl2. The combined organic layers were washed with saturated aqueous Na2CO3, water, brine and dried (Na2SO4). The solvent was removed under vacuum and the residue was purified on a silica gel column using light petroleum-ethyl acetate (4:1) as eluent to afford pure (2RS,6S)-2-benzenesulfonyl-6-(4-fluorophenoxymethyl)-tetrahydropyran (0.5 g, 70%) as a viscous liquid. TLC:ethyl acetate-light petroleum (1:3), Rf=0.4. 1H NMR (CDCl3, 200 MHz): δ 1.5 (m, 2H), 1.75-2.0 (m, 2H), 2.2-2.4 (m, 1H), 2.6-2.8 (m, 1H), 3.75-3.9 (m, 2H), 4.65 (d, 1H), 4.85-5.0 (m, 1H), 6.7-7.0 (m, 4H), 7.5-7.7 (m, 3H), 7.95 (d, J=5.4 Hz, 2H).
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-0943c4cb7cec459983a252db7faabcbc |
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| Source note | uspto-grants-2003_05 |
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