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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077128Generated: October 26, 2026

Sodium Hydroxide → Ketoamine 1-diethylamino-6-m-methoxyphenylhexan-3-one

https://huagongshe.com/reaction/1077128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1-Diethylamino-6-m-methoxyphenylhex-2-yneHCID 21485597—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
ProductKetoamine 1-diethylamino-6-m-methoxyphenylhexan-3-oneHCID 86733483—

Reaction Steps

Add mercuric sulphate (0.45 g) to a swirled solution of 1-diethylamino-6-m-methoxyphenylhex-2-yne (8.5 g) in concentrated sulphuric acid (2.5 cc) and water (25 cc). Keep the solution under nitrogen at 75°C for 1 hour, then cool, make basic with 10% aqueous sodium hydroxide, and filter through glass wool to remove mercuric oxide. Extract product with ether and wash and dry the ethereal solution. Remove the solvent to obtain the crude ketoamine 1-diethylamino-6-m-methoxyphenylhexan-3-one, infrared absorption peak at 1710 μ. Distil under reduced pressure with partial elimination of diethylamine, to obtain a mixture of the ketoamine 1-diethylamino-6-m-methoxyphenylhexan-3-one and the vinyl ketone 6-m-methoxyphenylhex-1-en-3-one (7.1 g, ca. 76%), b.p. 140°-145°C/0.1 mm; infrared absorption peaks at 5.85 and 5.95 μ, the ketoamine predominating.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03959322
Source datasetuspto-grants-1976_05
ORD IDord-3f2739b14015420fb89949abcd75d3d6
Source noteuspto-grants-1976_05