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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649514Generated: October 30, 2026

Water → 5-(Triphenylmethyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine

https://huagongshe.com/reaction/649514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
Reactant4,5,6,7-Tetrahydrothieno(3,2-c)pyridineHCID 3085076—
SolventDichloromethaneHCID 6344—
Product5-(Triphenylmethyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridineHCID 1374846196%

Reaction Steps

To a solution of 100 g (0.718 mole) of 4,5,6,7-tetrahydro thieno [3,2-c]pyridine in 200 ml of dichloromethane, are added 80 ml (0.789 mole) of triethylamine, then 200.2 g (0.718 mole) of triphenylmethylchloride is added, drop by drop, at ambient temperature. The reaction medium is left overnight at ambient temperature. The reaction medium is poured into 2000 ml of water. The organic phase is decanted, dried over sodium sulfate and evaporated to dryness. The residue is purified by filtration on a silica bed (elution with dichloromethane). The product is white crystals, M.P.=95° C. (pasty); yield: 96%; NMR 1H (in ppm) (CDC13): 7.57-6.90 (m, 15H); 6.80 (c, J =6.5 Hz, 1H); 6.43 (d, J=6.5 Hz, 1H); 3.35 (s, 14), 3.00-2.33 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04740510
Source datasetuspto-grants-1988_04
ORD IDord-6ababfb908b444dc96346b73166ec988
Source noteuspto-grants-1988_04