Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276341Generated: October 30, 2026

Hydrochloric Acid → HCID 178470750, compound

https://huagongshe.com/reaction/2276341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl SuccinateHCID 31249—
Reactant(2-Amino-4,5,6,7-tetrahydro-1-benzothien-3-yl)(4-methylphenyl)methanoneHCID 754850—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178470750HCID 17847075023.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of sodium ethoxide 21% in ethanol (1.8 mL; 4.8 mmol) in dry ethanol (30 mL) under a nitrogen atmosphere was added (2-amino-4,5,6,7-tetrahydrobenzo[b]thiophen-3-yl)(p-tolyl)methanone (1.09 g; 4 mmol) and diethyl succinate (0.929 mL; 5.6 mmol). The mixture was heated to 100° C. for 24 h. The reaction mixture was dissolved with water (8 ml) and acidified with a solution of hydrochloric acid 1N to pH 1 and the aqueous layer was extracted with ethyl acetate. The organics were combined, dried over sodium sulphate and concentrated under reduced pressure. The crude was suspended in dry ethanol (30 mL) and a catalytic amount of concentrated sulfuric acid (10 drops) was carefully added. The reaction mixture was heated to reflux for 21 h. The volatiles were removed under reduced pressure and the remaining residue was purified by flash-chromatography on silica gel using a gradient of methanol (1-20%) in ethyl acetate as eluent to furnish 0.358 g (19.6%) of ethyl[2-hydroxy-4-(p-tolyl)-5,6,7,8-tetrahydro[1]benzothieno[2,3-b]pyridin-3-yl]acetate as an ochre solid. ESI/APCI(+): 382 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09132129B2
Source datasetuspto-grants-2015_09
ORD IDord-96a11ca33be04fd4ae7d4ae722a7f6d9
Source noteuspto-grants-2015_09