HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899277Generated: October 29, 2026
HCID 22640688, compound → HCID 22640670, compound
https://huagongshe.com/reaction/899277
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22640688 | HCID 22640688 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22640670 | HCID 22640670 | — |
Reaction Steps
A suspension of methyl triphenylphosphonium bromide (2.293 g, 6.42 mmole) in 40 mL of THF at 0° C., was treated dropwise with 2.6 mL of 2.5M butyllithium. The mixture was stirred at room temperature for 30 minutes and then cooled to 0° C. A solution of 1-(4,4-dimethyl-thiochroman-7-yl)-hexan-1-one (1.183 g, 4.28 mmole) in 10 mL of THF was added to the ylide solution. The reaction mixture was stirred at room temperature for one hour, quenched by the addition of 50 mL water and was extracted with three 50 mL portions of ether. The combined organic extracts were dried over MgSO4, filtered and concentrated in vacuo to give a yellow solid. The product was purified by flash chromatography (SiO2, 1% ethyl acetate in hexanes) to yield 0.939 g of 4,4-dimethyl-7-(1-methylene-hexyl)-thiochroman as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07354931B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-7b7047c965a244f2921f3fcb732cd5d7 |
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| Source note | uspto-grants-2008_04 |
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