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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666111Generated: October 26, 2026

Dicyclohexylcarbodiimide → HCID 178477928, compound

https://huagongshe.com/reaction/1666111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant(R)-(-)-1-Indanyl isothiocyanateHCID 7018249—
Reactant(2-Amino-6-chlorophenyl)methanolHCID 21925574—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178477928HCID 17847792836%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a stirred solution of commercially available 2-amino-6-chlorobenzyl alcohol (CAS-no. 39885-08-0) (315 mg, 2 mmol) in tetrahydrofuran (4 ml) at 23° C. was added commercially available (R)-(−)-1-indanyl isothiocyanate (CAS-no. 737000-97-4) (324 ul, 2 mmol) and the mixture was stirred at 23° C. for 18 h, then at reflux for another 3 h. Cooled to 23° C., the solvent was removed in vacuum, the residue was dissolved in acetonitrile (4 ml), added dicyclohexylcarbodiimide (DCC) (619 mg, 3.0 mmol) and refluxed for 2 h. Cooled to room temperature, diluted with ethyl acetate and water, added little 1 M NaH2PO4.2H2O solution to achieve pH 4, separated phases, washed organic layer with brine and dried over sodium sulfate. Removal of the solvent in vacuum left a yellow foam, which was purified by silica gel flash chromatography with n-heptane and ethyl acetate to give the title compound as a light yellow oil (215 mg, 36%), MS (ISP) m/e=299.1 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044047B2
Source datasetuspto-grants-2011_10
ORD IDord-710910d8543640cc948fa21e170b7426
Source noteuspto-grants-2011_10