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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345300Generated: October 30, 2026

2-Aminothiophenol → HCID 86745158, compound

https://huagongshe.com/reaction/345300

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
ReactantHCID 54522509HCID 54522509—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 86745158HCID 8674515850%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 2-phenylmethyl-1-carboxymethylenecyclohexane (3.0 g) and 2-aminothiophenol (5.0 g) in N,N-dimethylformamide (3 ml) was refluxed for 20 hours under nitrogen atmosphere. The mixture was cooled to 0° C. and diluted with ethyl acetate (30 ml) and the mixture was washed with 1N hydrochloric acid (30 ml), water (30 ml), a saturated aqueous solution of sodium bicarbonate (30 ml) and brine (30 ml). The organic layer was dried over magnesium sulfate and concentrated in vacuo. The residue was triturated with diethyl ether to give 2'-phenylmethyl-4,5-dihydro-4-oxospiro[1,5-benzothiazepine-2(3H), 1'-cyclohexane] (2.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057513
Source datasetuspto-grants-1991_10
ORD IDord-c9fd4d5907274083b8b791c6e671dd01
Source noteuspto-grants-1991_10