Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740481Generated: October 30, 2026

Thionyl Chloride → HCID 14986648, compound

https://huagongshe.com/reaction/1740481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant6-{[tert-Butyl(dimethyl)silyl]oxy}hexanoic acidHCID 12717311—
SolventBenzeneHCID 241—
ProductHCID 14986648HCID 1498664892%

Reaction Steps

A solution of 0.5 g (2.03 mmol) of 6-[(tert-butyldimethylsilyl)oxy]-hexanoic acid in 4 ml of benzene is mixed with 362 mg (3.04 mmol, 1.5 equivalents) of SOCl2 and heated under reflux for 2 hours. It is allowed to cool, and the solvent is distilled off in a rotary evaporator. To remove excess SOCl2 from the reaction mixture, the residue is mixed again with benzene and again distilled off. 494 mg (1.865 mmol, 92%) of the 6-[(tert-butyldimethylsilyl)oxy]-hexanoyl chloride is obtained. This crude product is further reacted without purification and characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05969145
Source datasetuspto-grants-1999_10
ORD IDord-39bcfc28f2d84ced9c19de69e2b00cf0
Source noteuspto-grants-1999_10