Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 7-Octene-1,2-diol | HCID 565266 | — |
| Reactant | p-Anisyldiphenylmethyl chloride | HCID 14836583 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 8-Hydroxy-7-methoxy-1-octene | HCID 19939570 | 45.8% |
Reaction Steps
A mixture of 45 g of 7,8-dihydroxy-1-octene and 101.2 g of p-anisylchlorodiphenylmethane in 200 ml of pyridine was allowed to stand at 10° C. for 48 hours. the mixture was poured into water and extracted with ether. The ether solution was dried and evaporated. The residue was dissolved in 300 ml of dimethylformamide containing 83.1 ml of methyl iodide and this solution was added dropwise to a suspension of 17.75 g of 60% sodium hydride in 500 ml of dimethylformamide over a 2 hour period. After stirring an additional 13 hours the mixture was poured into water and extracted with ether. The ether solution was dried and evaporated. The residue was dissolved in 400 ml of methanol and stirred with 35 g of Amberlyst 15 resin. The solution was filtered and solvent was removed. The residue was purified by chromatography giving 22.6 g of 8-hydroxy-7-methoxy-1-octene as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05234918 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-cd9e7813ad7a42e1bd96ce9b703bf8f4 |
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| Source note | uspto-grants-1993_08 |
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