Thionyl Chloride → Cyclopentylmethanesulfonyl Chloride

HRID 397682Notes

Reaction equation

[CH:1]1([CH2:6][S:7]([O-:10])(=O)=[O:8])[CH2:5][CH2:4][CH2:3][CH2:2]1.[Na+].S(Cl)([Cl:14])=O>>[CH:1]1([CH2:6][S:7]([Cl:14])(=[O:10])=[O:8])[CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

Reactant 2

HCID 24386Thionyl Chloride

HCID 23670187Sodium cyclopentylmethanesulfonate

Product 1

HCID 2735404Cyclopentylmethanesulfonyl Chloride

Procedure

The subtitle compound was prepared by the method of Preparation 58 from sodium cyclopentylmethanesulfonate [Preparation 64] and thionyl chloride, to afford cyclopentylmethanesulfonyl chloride as a solid.

Sources & evidence

ORD record: ord-866d82d2a03c41c98c19c15a2187fd5a
Source dataset: uspto-grants-2003_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06610707B1

Reaction notes

Loading…