Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1,2-Epoxydecane | HCID 16993 | — |
| Product | 2-Decanol, 1-methoxy- | HCID 9990039 | — |
Reaction Steps
The same reactor that was used in Production Example 5 was charged with 64 g (2 mol) of methanol and 2 g of boron trifluoride diethyl ether complex and then the mixture was raised to 60° C. Then, 156.2 g (1 mol) of 1,2-epoxydecane was added dropwise to the mixture over one hour and the resulting mixture was kept as it was for 3 hours. The reaction was terminated just after confirming that 1,2-epoxydecane left unreacted was less than 1% by gas chromatography and then the reaction mixture was cooled. Thereafter, methanol was removed in the same manner as in Production Example 5 to obtain 2-hydroxydecyl methyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07135443B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-482326502bc84d87bb3b55dd970d3bc6 |
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| Source note | uspto-grants-2006_11 |
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