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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398588Generated: October 31, 2026

Water → HCID 70623127, compound

https://huagongshe.com/reaction/2398588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant4-Tert-ButylbenzenethiolHCID 75454—
ReactantHCID 21387104HCID 21387104—
SolventMethanolHCID 887—
ProductHCID 70623127HCID 70623127—

Reaction Steps

To a stirred solution of 4.96 grams (.062 moles) of 50% sodium hydroxide in 100 ml of methanol in a 250 ml erlenmeyer flask was added 10.45 grams (.063 moles) of para-(t-butyl)thiophenol and the solution stirred for 15 minutes at room temperature. The solution was cooled to 5° C. and 13.7 grams (.06 moles) of 1-cyclohexylazo-1-chlorocyclohexane (from Example 3-11) was added dropwise over 20 minutes while holding the reaction temperature at 5° to 10° C. with a cold water bath. After the addition was complete the bath was removed and the reaction stirred for an additional 60 minutes at room temperature. A 1.0 gram portion of 50% sodium hydroxide was then added to react with any excess thiophenol, the reaction mixture poured into 300 ml water and the product extracted into 100 ml of pentane. The pentane solution was separated and successively washed with 50 ml portions of water, 10% HCl, water, 5% sodium hydroxide and saturated sodium bicarbonate solution, dried over anhydrous sodium sulfate, filtered and the pentane evaporated under reduced pressure on a rotating evaporator. The product was a yellow liquid that weighed 14.0 grams (63% crude yield). The infrared spectrum of the product was in agreement with the structure of 1-cyclohexylazo-1-[para-(t-butyl)-thiophenoxy] cyclohexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04025502
Source datasetuspto-grants-1977_05
ORD IDord-109c4547026447449f37591ba78399ad
Source noteuspto-grants-1977_05