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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259348Generated: October 29, 2026

1-(Methoxymethyl)-3-(4,5,6,7-tetrahydro-7-hydroxybenzo[b]thien-4-yl)urea → 1-(Methoxymethyl)-3-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)urea

https://huagongshe.com/reaction/259348

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Methoxymethyl)-3-(4,5,6,7-tetrahydro-7-hydroxybenzo[b]thien-4-yl)ureaHCID 20348889—
CatalystHCID 178418406HCID 178418406—
SolventAcetoneHCID 180—
Product1-(Methoxymethyl)-3-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)ureaHCID 2034899090.7%

Reaction Steps

A solution of 1-(methoxymethyl)-3-(4,5,6,7-tetrahydro-7-hydroxybenzo[b]thien-4-yl)urea (0.35 g., 1.37 mmole) in acetone (40 ml.) is treated with manganese dioxide (3.5 g.). After 2 hours stirring the reaction mixture is filtered through celite, the cake washed thoroughly with acetone and the filtrate and washings evaporated to furnish 0.32 g. on 90.7% yield of the title compound as a crystalline solid, m.p. 155°-158° C. Recrystallization from hot acetone affords the analytical sample, m.p. 159°-162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04036979
Source datasetuspto-grants-1977_07
ORD IDord-9d1b3635fb0240128f7c10e519335d11
Source noteuspto-grants-1977_07