Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972136Generated: October 29, 2026

1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde → HCID 42635546, compound

https://huagongshe.com/reaction/1972136

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—
ReactantHCID 694901HCID 694901—
ProductHCID 42635546HCID 4263554667%

Reaction Steps

The condensing of commercially available 1-trityl-1H-imidazole-4-carboxaldehyde (I) with phtalide to form 2-(1-trityl-1H-imidazole-4-yl)indan-1,3-dione (II) is performed under the conditions that are similar to those used for synthesis of 4-(indane-1,3-dionyl)pyridine J. Org. Chem. 1971, vol. 36, p. 1563. surprisingly, the bulky 1-trityl-1H-imidazole-4-carboxaldehyde (I) reacted as expected and produced 2-(1-trityl-1H-imidazole-4-yl)indan-1,3-dione (II) in over 67% yield. Both ethyl acetate and dioxane can be used as reaction media.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431717B2
Source datasetuspto-grants-2013_04
ORD IDord-e4fdd5e23a5b418c82829c465e7583c9
Source noteuspto-grants-2013_04