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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254311Generated: November 3, 2026

Hydrochloric Acid → cis 5,6-dihydro-6-(2-ethoxycarbonylethyl)-4-(4-methoxybenzylamino)-4H-thieno[2,3-b]thiopyran

https://huagongshe.com/reaction/2254311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
Reactant4-MethoxybenzylamineHCID 75452—
ReactantSodium borohydrideHCID 4311764—
Reactant5,6-Dihydro-4-oxo-5-(2-ethoxycarbonylethyl)thieno[2,3-b]thiopyranHCID 67883166—
CatalystTitanium TetrachlorideHCID 24193—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Productcis 5,6-dihydro-6-(2-ethoxycarbonylethyl)-4-(4-methoxybenzylamino)-4H-thieno[2,3-b]thiopyranHCID 86747095—

Reaction Steps

To a solution of 2 (10.4 g, 0.039 mol) in THF (110 ml) and toluene (110 ml) at 0° is added 4-methoxybenzylamine (25.5 ml, 26.8 g, 0.195 mol). Titanium tetrachloride (2.2 ml, 3.8 g, 0.02 mol) is added to the cold solution and the resulting mixture is stirred for 0.75-1 hour. The mixture is added to a cold (0°) stirred suspension of NaBH4 (4.5 g, 0.12 mol) in EtOH (900 ml). The resulting mixture is stirred for about 1 hour and acidified to pH 1 with 3N HCl. The solvent is removed in vacuo and the residue partitioned between EtOAc and saturated NaHCO3 solution. The EtOAc layer is separated, dried and concentrated to dryness to yield 3 wherein R1, R2, R3 and R4 are each H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05235059
Source datasetuspto-grants-1993_08
ORD IDord-68e0aeaf7c0440b7bf7780fc3524c4be
Source noteuspto-grants-1993_08