Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Octanoic Acid | HCID 379 | — |
| Reactant | 1,6-Hexanediol | HCID 12374 | — |
| Reactant | HCID 23036666 | HCID 23036666 | — |
| Product | HCID 54500825 | HCID 54500825 | — |
Reaction Steps
A mixture of caprylic acid (110.5 g; 0.7662 mol) and 1,6-hexandiol (600 g; 5.077 mol) was heated to max. temperature 200° C. for 5 hours, while 25 g of organic volatile compounds and water was removed by distillation. The excess of 1,6-hexandiol was distilled off in vacuum and the residue was cooled and diluted with benzene (750 ml). The benzene solution was extracted with water (3×250 ml), the solvent was evaporated, and the product was distilled through a short empty column (100×25 mm). 6-Hydroxyhexyl caprylate (HHC) had b.p. 120° C./8 Pa. The main fraction containing 98.6% HHC was obtained in the yield of 157.2 g (84%). Elemental analysis for C14H28O3 theory: 68.81% C; 11.55% H; found: 68.65% C, 11.72% H. Infrared and 13C--NMR spectra proved the structure of HHC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04950733 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-03f97dcaa43a424e832844d420b2d8c3 |
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| Source note | uspto-grants-1990_08 |
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