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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410395Generated: November 2, 2026

Octanal → HCID 10103696, compound

https://huagongshe.com/reaction/2410395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOctanalHCID 454—
ReactantHCID 178455850HCID 178455850—
SolventDiethyl EtherHCID 3283—
ProductHCID 10103696HCID 1010369660%

Reaction Steps

To a solution of 1.2 mL (7.8 mmol) of octanal in 30 mL of ether was added 15.6 mL of a 1.0 M solution of allylmagnesium bromide in ether. The reaction was allowed to stir at room temperature for 18 h and then quenched with saturated NH4Cl. The product was extracted with ether (2×20 mL), dried over Na2SO4 and filtered. The solvent was removed under reduced pressure and the remaining residue was purified by flash chromatography to give 0.79 g (60%) of the allylic alcohol. 1H NMR (400 MHz, CDCl3) δ 5.80-5.70 (m, 1H), 5.04-4.99 (m, 2H), 3.53 (m, 1H), 2.52 (br s, 1H), 2.20-2.05 (m, 2H), 1.381-34 (m, 2H), 1.25-1.15 (m, 10H), 0.80 (t, J=7.1 Hz, 3H); 13C NMR (400 MHz, CDCl3) δ 133.6, 116.3, 70.6, 42.5, 37.5, 32.7, 30.6, 30.2, 26.7, 23.7, 15.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816095B2
Source datasetuspto-grants-2014_08
ORD IDord-c55eb9becaf043f7980c37db62da96d8
Source noteuspto-grants-2014_08