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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847478Generated: October 25, 2026

tert-Butanol → HCID 11770349, compound

https://huagongshe.com/reaction/847478

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantAmmonium ChlorideHCID 25517—
ReactantCyclopentyltrimethoxysilaneHCID 9855701—
ReactantPotassium tert-butoxideHCID 23665647—
ProductHCID 11770349HCID 1177034921%

Reaction Conditions

Temperature80 °C

Reaction Steps

In a 100 ml three-neck flask provided with a magnetic stirrer and a reflux condenser were charged 25.0 g (0.131 mole) of cyclopentyl trimethoxysilane, 9.74 g (0.131 mole) of tert.-butyl alcohol and 20 mg (0.18 m mole) of potassium tert.-butoxide, which were then reacted with each other by heating under stirring in an oil both of 80° C. for 10 hours. After cooled, ammonium chloride was added to neutralize the alkali. Then, tert.-butoxy cyclopentyl dimethoxysilane of 6.25 g (0.0269 mole) was obtained by vacuum distillation. Its structure was confirmed as in Example 1. The yield was 21%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05142082
Source datasetuspto-grants-1992_08
ORD IDord-79a65caf01b946a0b3ea613c70124241
Source noteuspto-grants-1992_08