HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899270Generated: October 28, 2026
HCID 22640671, compound → 4,4-Dimethyl-7-(1-methylene-hexyl)-chroman
https://huagongshe.com/reaction/899270
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 22640671 | HCID 22640671 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,4-Dimethyl-7-(1-methylene-hexyl)-chroman | HCID 22640681 | — |
Reaction Steps
A suspension of methyl triphenylphosphonium bromide (1.062 g, 2.97 mmole) in 20 mL of THF at 0° C. was treated dropwise with 1.2 mL of a 2.5M butyllithium solution. The mixture was stirred at room temperature for 30 minutes and then cooled to 0° C. A solution of 1-(4,4-dimethyl-chroman-7-yl)-hexan-1-one (0.516 g, 1.98 mmole) in 5 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 25 mL water and extracted with three 25 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, 2% ethyl acetate in hexanes) to yield 0.442 g of 4,4-dimethyl-7-(1-methylene-hexyl)-chroman 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-498240b365534b988f537046904b4870 |
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| Source note | uspto-grants-2008_04 |
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