Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Naphthalene | HCID 931 | — |
| Reactant | Hexanal | HCID 6184 | — |
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | Lithium Naphthalene | HCID 57466756 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Decyn-5-ol | HCID 21518441 | — |
Reaction Steps
Following the procedure of Example 1, but with a pressure equalizing dropping funnel in place of the gas addition tube, 100 g. of naphthalene (0.77 moles) were added to 7.3 g. of lithium metal powder (1.05 moles) in 100 ml. tetrahydrofuran forming a dark green-brown lithium-naphthalene adduct over a period of about 30 minutes. 168 g. of the gaseous hydrocarbon mixture of Example 1 dissolved in 800 ml. tetrahydrofuran were added to the flask over a two hour period while maintaining the slurry at a temperature of about 55°C. Near the end of the addition, the slurry turned to an olive green color and became light brown after stirring for an additional hour. An aliquot of the resultant product was reacted with 1-hexanal producing 3-decyn-5-ol which, by gas chromotograph analysis, establishes a yield of butynyllithium in excess of 90%, based on lithium.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03975453 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-d74eaf3fba7c4b948c3ead48196f2dd8 |
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| Source note | uspto-grants-1976_08 |
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