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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059271Generated: October 30, 2026

Acetic Anhydride → 3-[2-Acetamido-4-dimethylaminophenyl]-3-(1-ethyl-2-methyl-3-indolyl)-4,5,6,7-tetrachlorophthalide

https://huagongshe.com/reaction/2059271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantN,N-dimethyl-m-phenylenediamineHCID 76084—
Reactant1-Ethyl-2-methyl-3-(2-carboxy-3,4,5,6-tetrachlorobenzoyl)indoleHCID 19763805—
Product3-[2-Acetamido-4-dimethylaminophenyl]-3-(1-ethyl-2-methyl-3-indolyl)-4,5,6,7-tetrachlorophthalideHCID 20523548—

Reaction Steps

Proceeding in a manner similar to that described in Example 13 above, 4.43 g (0.01 mole) of 2-[(1-ethyl-2-methyl-3-indolyl)carbonyl]-3,4,5,6-tetrachlorobenzoic acid, prepared as described in Example 2, part A above, was interacted with 2.0 g (0.015 mole) of m-amino-N,N-dimethylaniline in the presence of ten ml of acetic anhydride to obtain 3-[2-acetamido-4-dimethylaminophenyl]-3-(1-ethyl-2-methyl-3-indolyl)-4,5,6,7-tetrachlorophthalide (Formula III: R°=R1 =R2 =R3 =Cl; R=R5 =CH3 ; ##STR34## R6 =CH2CH3 ; Y1H) which developed a blue-green color when spotted on silica gel in the form of a toluene solution.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04322352
Source datasetuspto-grants-1982_03
ORD IDord-9569116ca3ed4f638a58f7e83d9e5073
Source noteuspto-grants-1982_03