Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Octanol | HCID 957 | — |
| Reactant | 3-Chloro-1,2-propanediol | HCID 7290 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86594669 | HCID 86594669 | — |
Reaction Steps
23 g (1 mol) of sodium were added in portions over the course of 4 hours to 325 g (2.5 mol) of 1-octanol while stirring at 105° C. (the temperature did not rise above 120° C. during this). The mixture was stirred at 115° C. for 1 hour. Subsequently, 110.5 g (1 mol) of 3-chloro-propane-1,2-diol were added over the course of 2 hours, and the mixture was stirred at 120° C. for 3 hours. After cooling, the mixture was taken up in 400 ml of diethyl ether and extracted 3× with a total of 700 ml of water. The ethereal phase was dried over sodium sulphate and concentrated. The residue was distilled in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07481973B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-b8b3502450b54c19bc3847a68e635c3e |
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| Source note | uspto-grants-2009_01 |
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