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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866741Generated: October 30, 2026

Acetate → HCID 86735853, compound

https://huagongshe.com/reaction/866741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
ReactantPhenolHCID 996—
ReactantPhosgeneHCID 6371—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Tert-ButylbenzenethiolHCID 75454—
ReactantCarbonochloridateHCID 21226386—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
SolventPentaneHCID 8003—
ProductHCID 86735853HCID 86735853—

Reaction Steps

This compound was prepared in the same manner as the 4-phenoxy derivative described in Example XXIX except p-t-butylthiophenol was added instead of phenol to the methanolic solution of KOH before the chloro compound was added in step C. The acetate was saponified to the alcohol by the addition of excess base to the methanol after the reaction of the chloro compound and the p-t-butylthiophenol was complete. The alcohol was then converted to the chloroformate by adding a pentane solution of the alcohol and pyridine to a pentane solution of phosgene as in step D of Example XXIX. The infrared spectrum confirmed that the alcohol was converted to the chloroformate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04101522
Source datasetuspto-grants-1978_07
ORD IDord-8b13ca1dd39545948405a4218acbc83a
Source noteuspto-grants-1978_07