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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583785Generated: October 25, 2026

Ammonia → HCID 53968399, compound

https://huagongshe.com/reaction/583785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTrifluoromethanesulfonyl chlorideHCID 79000—
Reactant1,1'-ThiocarbonyldiimidazoleHCID 80264—
ReactantCID 66729449HCID 66729449—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53968399HCID 53968399—

Reaction Steps

To a stirred solution of 1,1′-thiocarbonyldiimidazole (0.01 mol), in THF is added sodium benzyloxide (0.01 mol), and the mixture is stirred for from 1 minute to about 24 hours. To the mixture is added ammonia gas, and the mixture is stirred at atmospheric pressure or shaken at from atmospheric pressure to about 75 psi. Reaction progress may be followed by TLC or HPLC. (Alternatively, the imidazolyl leaving groups may be first activated (sequentially) by sulfonylation on nitrogen by pretreatment before each displacement with a suitable sulfonylating reagent such as trifluoromethanesulfonyl chloride or para-toluenesulfonyl chloride. This allows displacement of imidazolyl under less rigorous reaction conditions.) When a sufficient amount of desired product is formed, the mixture is partitioned between ethyl acetate and water, or optionally the mixture is first rotary evaporated, and the residue is so partitioned. The organic layer is washed with brine, dried over sodium sulfate, and rotary evaporated to give thiocarbamic acid, benzyl ester, which may be purified, if needed or desired, by chromatography on silica gel or crystallization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924276B2
Source datasetuspto-grants-2005_08
ORD IDord-5ee33573299b4b2eb3ad8b353fc6e015
Source noteuspto-grants-2005_08