HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62560Generated: October 25, 2026
9-Decen-1-ol → Dec-9-en-1-yl oct-7-enoate
https://huagongshe.com/reaction/62560
Participants
| Role | Name | HCID | Charge |
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| Reactant | 9-Decen-1-ol | HCID 25612 | — |
| Reactant | 7-Octenoic acid | HCID 543977 | — |
| Product | Dec-9-en-1-yl oct-7-enoate | HCID 71526901 | — |
Reaction Steps
Following the aforementioned procedure, diene was prepared from oct-7-enoic acid and dec-9-en-1-ol. The resulting yellow oil was purified by silica gel chromatography (50:1 hexanes: diethyl ether) to afford the desired product as a colorless oil. IR (neat): 3077 (m), 2926 (s), 2855 (s), 1736 (s), 1641 (m), 1462 (m), 1417 (m), 1351 (m), 1255 (s), 1168 (s), 1113 (m), 1076 (m), 993 (s), 909 (s), 734 (m), 632 (m); 1H NMR (400 MHz, CDCl3): δ 5.86-5.75 (2H, m), 5.02-4.91 (4H, m), 4.05 (2H, t, J=6.8 Hz), 2.29 (2H, t, J=7.6 Hz), 2.08-2.01 (4H, m), 1.67-1.59 (4H, m), 1.42-1.27 (14H, m); 13C NMR (100 MHz, CDCl3): δ 174.0, 139.2, 138.9, 114.5, 114.3, 64.5, 34.4, 33.9, 33.7, 29.5, 29.3, 29.1, 29.0, 28.8, 28.7, 28.6, 26.0, 25.0; HRMS (ESI+) [M+H]+ calcd for C18H33O2: 281.2481. found: 281.2475.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09446394B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-bea07f6834b246709e68d46c3e258aa2 |
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| Source note | uspto-grants-2016_09 |
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