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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074002Generated: November 1, 2026

Acetic Acid → 1-Acetyl-5-carbomethoxy-7-chloro-4-methoxy-1,2-dihydroindole

https://huagongshe.com/reaction/2074002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-Acetyl-5-carbomethoxy-7-chloro-4-methoxyindoleHCID 10493103—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
Product1-Acetyl-5-carbomethoxy-7-chloro-4-methoxy-1,2-dihydroindoleHCID 10564950—

Reaction Steps

The mixture of the indole of step 8 above (0.9 g) and Pt-C (0.2 g), acetic acid and MeOH (100 ml) is stirred under H2 at 1 atm. pressure for 48 hours. The catalyst is filtered (celite), the filtered material is washed (MeOH) and the reaction mixture and methanol washings are evaporated. The residue is diluted with CH2Cl2, washed with saturated NaHCO3, dried (MgSO4) and evaporated affording a colorless, semicrystalline material which is determined to be the desired compound by NMR. M.P. 107°-109° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04920219
Source datasetuspto-grants-1990_04
ORD IDord-be1d126f7a2a4da2bef77007ed389b1e
Source noteuspto-grants-1990_04