Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225883Generated: October 30, 2026

Quinone → methyl 5-hydroxy-2-(methoxymethyl)-1-methylindole-3-carboxylate

https://huagongshe.com/reaction/2225883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinoneHCID 4650—
ReactantHCID 85255412HCID 85255412—
SolventAcetic AcidHCID 176—
Productmethyl 5-hydroxy-2-(methoxymethyl)-1-methylindole-3-carboxylateHCID 1019883522%

Reaction Steps

3.1 g of 1,4-benzoquinone (28.7 mmol) was dissolved in 50 ml of acetic acid to which was subsequently added dropwise 2.28 g (14.3 mmol) of methyl 4-methoxy-3-methylamino-2-butenoate and the mixture was stirred for 5 hours at room temperature. After the solvent was distilled off under reduced pressure, the resulting residue was dissolved in ethyl acetate, washed with water and saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. After anhydrous magnesium sulfate was filtered off and the solvent was distilled off under reduced pressure, the residue was purified by a silica gel column chromatography (eluent: hexane-ethyl acetate, 2:1) to obtain 0.78 g of the title compound with a yield of 22%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344938
Source datasetuspto-grants-1994_09
ORD IDord-3523da35b3784fbbb29d60e458d8d907
Source noteuspto-grants-1994_09