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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082201Generated: October 30, 2026

Pyridine → HCID 15044334, compound

https://huagongshe.com/reaction/2082201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Methyl-2-butanolHCID 6405—
ReactantHCID 15917599HCID 15917599—
SolventDichloromethaneHCID 6344—
ProductHCID 15044334HCID 15044334—

Reaction Steps

One hundred ml of dichloromethane and 20.27 g (0.1 mol) of p-methylthiophenyl chloroformate prepared in the same manner as in Example 1 were placed in a flask, and 50 ml of a dichloromethane solution containing 8.15 g (0.1 mol) of tertamyl alcohol and 8.70 g (0.11 mol) of pyridine was dropped thereto at room temperature. The resulting mixture was then stirred for two hours. The reaction solution was washed with water to remove pyridine hydrochlorate, and the organic layer was concentrated under reduced pressure. Finally excessive pyridine was removed in vacuum whereupon 5.09 g of the desired product, tert-amyl p-methylthiophenyl carbonate was obtained as an oily material (yield 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05187311
Source datasetuspto-grants-1993_02
ORD IDord-3d76a7ca52104e1e8fc6034e75433416
Source noteuspto-grants-1993_02