Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Butanediol | HCID 8064 | — |
| Reactant | 1-Bromotridecane | HCID 13000 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Product | 4-Tridecyloxybutanol | HCID 20462324 | — |
Reaction Steps
2.3 g. Sodium are dissolved by warming in 44 ml. butane-1,4-diol, 38 ml. 1-bromotridecane are added thereto and the reaction mixture is stirred for 5 hours at a bath temperature of 150° C. After cooling, extraction is carried out with a mixture of diethyl ether-ligroin (1:2 v/v), the extract is evaporated and the residue is purified on a silica gel column by elution with ligroin which is subsequently replaced by diethyl ether-ligroin (1:1 v/v). The desired fractions are collected and evaporated. 19.4 g. (71% of theory) of thin layer chromatographically uniform 4-tridecyloxybutanol are thus obtained; m.p. 26°-29° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04444766 |
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| Source dataset | uspto-grants-1984_04 |
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| ORD ID | ord-7885c4defce94df783299bf51313dffd |
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| Source note | uspto-grants-1984_04 |
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