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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578812Generated: November 2, 2026

Sodium hydride → HCID 53830096, compound

https://huagongshe.com/reaction/1578812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 53963170HCID 53963170—
ReactantHCID 54451904HCID 54451904—
SolventDiethyl EtherHCID 3283—
ProductHCID 53830096HCID 5383009696.2%

Reaction Steps

To a suspension of sodium hydride (2.64 g) in ether (70 ml), a solution of ethyl 3,7,11-trimethyl-6,10-dodecadien-2-one-1-carboxylate (14.7 g) in ether (15 ml) is dropwise added, and then a solution of 1-bromo-8-acetoxy-2,6-dimethyl-2,6-octadiene (15 g) in ether (15 ml) is dropwise added thereto while cooling with ice. The reaction mixture is poured into ice water. The ether layer is washed with water, dried and evaporated. The residue (24.8 g) is added to a solution of potassium hydroxide (8.4 g) in ethanol (150 ml), and the resultant mixture is poured into water, followed by washing with petroleum ether, acidifying with 5% aqueous solution of sulfuric acid and extracting with ether. The ether layer is washed with water, dried and evaporated. The resulting product (23.5 g) is purified by chromatography on silica gel (235 g) using benzene to give 3,7,11,15,19-pentamethyl-2,6,14,18-eicosatetraen-10-on-1-ol (18 g). IR: 3400, 1000 cm-1 (OH): 1705 cm-1 (C=O); 1668 cm-1 (C=C). NMR (carbon tetrachloride): δ 1.04 (d), 1.59 (s), 1.66 (s), 2.01 (m), 2.7 (m), 4.1 (m), 5.05 (m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03939202
Source datasetuspto-grants-1976_02
ORD IDord-5ec1d810650d4936bc66d09951eab4f6
Source noteuspto-grants-1976_02