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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385190Generated: October 30, 2026

Hydrochloric Acid → HCID 178525719, compound

https://huagongshe.com/reaction/385190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantCarbon DisulfideHCID 6348—
ReactantTriethylamineHCID 8471—
ReactantHCID 178511262HCID 178511262—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178525719HCID 178525719101%

Reaction Steps

Carbon disulfide (0.26 mL, 4.4 mmol) was added to a mixture comprising trans-4-(aminomethyl)cyclohexanecarboxylic acid (0.24 g, 1.5 mmol), tetrahydrofuran (1.0 mL), water (1.0 mL) and triethylamine (0.51 mL, 3.6 mmol), followed by stirring at room temperature for 44 hours. The obtained reaction mixture was dropwise added to a tetrahydrofuran (1.0 mL) solution of iodine (0.41 g, 1.6 mmol) over a period of 5 minutes at 0° C., followed by stirring at 0° C. for further two hours. Thereafter, 1M hydrochloric acid (1.5 mL) was added and mixed. Then, ethyl acetate (6 mL) was added, and the organic layer was separated and concentrated under reduced pressure to dryness. To the obtained residue, a solvent mixture of hexane (3 mL) and ethyl acetate (3 mL) was added and thoroughly mixed, and the insoluble matter was filtered off. Then, the filtrate was concentrated under reduced pressure to dryness to obtain trans-4-(isothiocyanatomethyl)cyclohexanecarboxylic acid as a ocher solid (0.30 g, yield: 101%, and 1H-NMR spectrum showed no distinct by-product). LC-MS ES-198(retention time: 20.3 min, condition 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367857B2
Source datasetuspto-grants-2013_02
ORD IDord-dfb536943b4f446a9e67345cb905f9d1
Source noteuspto-grants-2013_02