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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074003Generated: October 31, 2026

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

https://huagongshe.com/reaction/2074003

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Acetyl-5-carbomethoxy-7-chloro-4-methoxy-1,2-dihydroindoleHCID 10564950—
SolventSodium hydroxide methanolHCID 23721981—
Product1-Acetyl-5-carboxy-7-chloro-4-methoxy-1,2-dihydroindoleHCID 14883226—

Reaction Steps

A mixture of the indole ester of step 9 above (0.8 g) and 10% aqueous NaOH/MeOH (20 ml/80 ml) is stirred under reflux for 2 hours. The reaction mixture is concentrated and the aqueous residue is diluted with water and extracted with CHCl3. The organic layer is dried (MgSO4) and evaporated affording an off-white solid which is determined to be the desired compound by NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04920219
Source datasetuspto-grants-1990_04
ORD IDord-2d6adf4bd802410b97733c9b3797b538
Source noteuspto-grants-1990_04