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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703228Generated: November 1, 2026

1,3-Benzenediamine, N1,N1,N3,N3-tetramethyl- → HCID 20523575, compound

https://huagongshe.com/reaction/1703228

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Benzenediamine, N1,N1,N3,N3-tetramethyl-HCID 89715—
ReactantHCID 20523570HCID 20523570—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 20523575HCID 20523575—

Reaction Steps

A mixture of 0.34 g (0.001 mole) of 2-[(1,2-dimethyl-3-indolyl)carbonyl]-5-dimethylaminobenzoic acid prepared as described in Example 1 of U.S. Pat. No. 3,540,910 was interacted with 0.16 g (0.001 mole) of N,N,N',N'-tetramethyl-m-phenylenediamine in 5 ml of acetic anhydride in a similar manner to the procedure described in Example 1, part C hereinabove to obtain 3-[2,4-bis(dimethylamino)phenyl]-3-(1,2-dimethyl-3-indolyl)-6-dimethylaminophthalide (Formula III: R0 =R1 =R3 =Y1 =H; R2 =N(CH3)2 ; R=R5 =R6 =CH3 ; R4 =N(CH3)2) which melts over the range of 146°-152° C. A significant infrared absorption maximum appeared at 1760 cm-1 (C=O; s). A toluene solution of this product spotted on silica gel developed an intense grape-red-colored image.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04351768
Source datasetuspto-grants-1982_09
ORD IDord-77b0442af08742bc9bf59c4a2b789def
Source noteuspto-grants-1982_09