HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569672Generated: October 30, 2026
Hydrochloric Acid → HCID 112438, compound
https://huagongshe.com/reaction/569672
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,3-Benzenediamine, N1,N1,N3,N3-tetramethyl- | HCID 89715 | — |
| Reactant | 1(3H)-Isobenzofuranone, 6-(dimethylamino)-3-[4-(dimethylamino)phenyl]- | HCID 93693 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 112438 | HCID 112438 | — |
Reaction Steps
A mixture of 6.0 g of 3-(4-dimethylaminophenyl)-6-dimethylaminophthalide prepared as described in part A above, 100 ml of water, 3.5 g of N,N,N',N'-tetramethyl-m-phenylenediamine and 1.8 g of flake potassium hydroxide was heated at reflux with stirring for a period of approximately eighteen hours and then allowed to cool to room temperature. The resultant solution was made slightly acidic by the addition of ten percent aqueous hydrochloric acid causing a cream-colored solid to precipitate. The solid was collected by filtration, washed with water and air dried at 40° C. to obtain 2-[2,4,4'-tris(dimethylamino)benzhydryl]-5-dimethylaminobenzoic acid (Formula III: R=CH3 ; X=H; Y=4-(CH3)2NC6H4 ; Z=2,4-[(CH3)2N]2C6H3) as a slightly sticky, cream-colored solid melting over the range 119°-121° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04732991 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-9fe5709ab00f4603aa08567490ac11e6 |
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| Source note | uspto-grants-1988_03 |
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