Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-Decen-1-olHCID 25612—
Reactant7-Octenoic acidHCID 543977—
ProductDec-9-en-1-yl oct-7-enoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09446394B2
Source datasetuspto-grants-2016_09
ORD IDord-bea07f6834b246709e68d46c3e258aa2
Source noteuspto-grants-2016_09