HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550238Generated: October 30, 2026
Dimethyl Sulfide → HCID 11626638, compound
https://huagongshe.com/reaction/550238
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 67156466 | HCID 67156466 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11626638 | HCID 11626638 | 46% |
Reaction Steps
Under a nitrogen atmosphere, dimethylsulfide (1.72 ml) and a boron trifluoride-diethyl ether complex (0.86 ml, 6.8 mmol) were added to a solution of (3R,4R,5S,6R)-3,4,5-trisbenzyloxy-6-benzyloxymethyl-2-[3-(5-fluorobenzo[b]-thiophen-2-ylmethyl)naphthalen-1-yl]tetrahydropyran (550 mg, 0.68 mmol) in methylene chloride (15 ml) under cooling with ice. The reaction mixture was stirred at room temperature for 2.5 days, then a saturated sodium hydrogen carbonate aqueous solution was added under cooling with ice and the mixture was extracted with methylene chloride. The organic layer was washed with a saturated sodium chloride aqueous solution and then dried with sodium sulfate, and thereafter the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography [developing solution=methylene chloride:methanol (40:1)] to obtain the title compound (140 mg, 46%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943748B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-66369d874b4741948880cc3e35b0a4f9 |
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| Source note | uspto-grants-2011_05 |
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