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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637508Generated: October 30, 2026

Acetic Acid → HCID 19348732, compound

https://huagongshe.com/reaction/1637508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantSodium CyanideHCID 8929—
ReactantHCID 19348580HCID 19348580—
CatalystHCID 178418406HCID 178418406—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 19348732HCID 1934873288.1%

Reaction Steps

2.66 g (54.3 mmol) of sodium cyanide, 37.78 g (434.4 mmol) of manganese dioxide and 979 mg (16.3 mmol) of acetic acid were added to a solution of 3.35 g (10.9 mmol) of 3-(2,4-dimethoxy-5-formylphenyl)octanoic acid (prepared as described in Preparation 32) in 70 ml of methanol, and the resulting mixture was stirred for 4 hours. At the end of this time, the reaction mixture was acidified with 1 N aqueous hydrochloric acid and filtered using a Celite (trade mark) filter aid. The filtrate was then concentrated by evaporation under reduced pressure, and the concentrate was mixed with a small amount of water, after which it was extracted with ethyl acetate. The extract was washed with water and with a saturated aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure, and the resulting residue was purified by column chromatography through 100 g of silica gel, using a gradient elution method, with mixtures of ethyl acetate and methanol ranging from 50:0 to 50:3 by volume as the eluent, to give 3.25 g (yield 88%) of the title compound, melting at 106-107° C. (from ethyl acetate-hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06040339
Source datasetuspto-grants-2000_03
ORD IDord-199ff360555f49ecbb8409c7efc97daa
Source noteuspto-grants-2000_03