HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221937Generated: October 30, 2026
Sulfuryl chloride → HCID 68508325, compound
https://huagongshe.com/reaction/221937
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 68503973 | HCID 68503973 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68508325 | HCID 68508325 | 43.1% |
Reaction Steps
(3′R,4′S,5S,5′S,6′R)-3′,4′,5′-tris-benzyloxy-6′-benzyloxymethyl-3-[(4-ethylphenyl)methyl]-3′,4′,5′,6′-tetrahydro-2-trimethylsilyl-spiro[thieno[2,3,f]isobenzofuran-5(7H),2′-[2H]pyran] (0.122 g, 0.139 mmol) was dissolved in acetonitrile (0.93 mL). Sulfuryl chloride (20.6 mg, 0.153 mmol) was added to the resultant solution, and then the solution was stirred for 3.5 hours at room temperature. Saturated aqueous sodium hydrogen carbonate was added thereto, and the resultant mixture was extracted with ethyl acetate. The organic layer was concentrated under reduced pressure, and the resulting residue was purified by silica gel flash column chromatography (developing solution=ethyl acetate:n-hexane (1:11.5)), to thereby obtain the titled compound (50.2 mg, 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207134B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-a37abb554813427cb2a4b93628e52cbb |
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| Source note | uspto-grants-2012_06 |
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