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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290230Generated: October 29, 2026

2-methylthiophene-3-carbaldehyde → HCID 10526927, compound

https://huagongshe.com/reaction/1290230

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-methylthiophene-3-carbaldehydeHCID 529398—
Reactant4-Iodo-1-tritylimidazoleHCID 618252—
ReactantHCID 178461630HCID 178461630—
SolventDichloromethaneHCID 6344—
ProductHCID 10526927HCID 10526927—

Reaction Steps

To a solution of N-trityl-4-iodo-imidazole (11.8 g, 27 mmol) in dry CH2Cl2 (75 mL) was added EtMgBr (10.0 mL, 3.0M in Et2O) and the solution was stirred for 3 hrs. Then a solution of 2-methylthiophene-3-carboxaldehyde (3.3 g, 27 mmol) in CH2Cl2 (20 mL) was added and the reaction mixture was stirred at room temperature overnight. The reaction was quenched with NH4Cl (aq) and the mixture was transferred to a separatory funnel. The aqueous layer was extracted with a second portion of CH2Cl2. The extracts were combined and washed with a small portion of water, dried (Na2SO4), and filtered. The solvent was evaporated in vacuo to give a thick syrup which was triturated with Et2O to give a solid which was recrystallized with charcoal treatment from EtOAc to give (2-methylthien-3-yl)-1-trityl-imidazol-4-yl-methanol, B1. 1H NMR (CDCl3) supported the assigned structure. ##STR36##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750720
Source datasetuspto-grants-1998_05
ORD IDord-6ff6bc4e397d412e8909cdc1bff22a95
Source noteuspto-grants-1998_05