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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372586Generated: October 31, 2026

tert-Butyl isothiocyanate → HCID 53716090, compound

https://huagongshe.com/reaction/372586

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl isothiocyanateHCID 11544—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 14037275HCID 14037275—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 53716090HCID 53716090—

Reaction Steps

To a suspension of α-acetamido-p-aminophenylacetic acid (1.04 g, 5 mmol) in water (5 ml) was added 10% NaOH until solution was effected. The solution was diluted with an equal volume of ethanol and then t-butyl isothiocyanate (1.64 g, 15 mmol) in ethanol was added. The reaction was stirred at room temperature overnight and then refluxed 24 hours. The ethanol was evaporated in vacuo and the aqueous phase was acidified and filtered. The aqueous filtrate was extracted with ethyl acetate. The dried extracts were evaporated to give α-acetamido-p-(3-t-butylthioureido)phenylacetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04091227
Source datasetuspto-grants-1978_05
ORD IDord-8ce5e191eb404c668782ab77d462b820
Source noteuspto-grants-1978_05