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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473228Generated: November 1, 2026

Carbon Disulfide → 3-(4,4'-Dimethoxytrityloxymethyl)benzyl isothiocyanate

https://huagongshe.com/reaction/473228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantTriethylamineHCID 8471—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant3-(4,4'-Dimethoxytrityloxymethyl)benzylamineHCID 67253478—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthanolHCID 702—
Product3-(4,4'-Dimethoxytrityloxymethyl)benzyl isothiocyanateHCID 86671514—

Reaction Steps

3-(4,4′-Dimethoxytrityloxymethyl)benzylamine (5) (613 mg, 1.39 mmol), carbon disulfide (0.85 mL, 13.9 mmol, 10 eq.), and triethylamine (0.20 mL, 1.39 mmol) were dissolved in EtOH (2 mL). The air was evacuated from the reaction system, and then Ar was charged therein. The reaction mixture was stirred for 2 hours at a room temperature. Then, in an ice bath, to the mixture were added dropwise a solution of di-tert-butyl dicarbonate (3.06 mg, 1.40 mmol) in EtOH (0.6 mL) and a solution of DMAP (6.12 mg, 6 mol %) in EtOH (0.6 mL). The mixture was further stirred for 4 hours at a room temperature. TLC was used to confirm there was no starting material in the mixture. Then, the reaction mixture was evaporated under reduced pressure. The residue was purified by column chromatography (Hex:EtOAc=10:1) to isolate

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633304B2
Source datasetuspto-grants-2014_01
ORD IDord-7d780b52f8d847259b6fa272c4609f83
Source noteuspto-grants-2014_01