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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166047Generated: October 30, 2026

Thionyl Chloride → HCID 14990630, compound

https://huagongshe.com/reaction/2166047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 14990599HCID 14990599—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14990630HCID 1499063088.3%

Reaction Steps

To a stirred solution of 6.5 parts of 1-butyl-α-(3-chlorophenyl)-1H-benzotriazole-6-methanol in 45 parts of tetrahydrofuran were added 3.7 parts of thionyl chloride at room temperature. After stirring for 1 hour, the reaction mixture was concentrated. The product was extracted with ethyl acetate. The extract was washed with a diluted sodium hydrogen carbonate solution, dried, filtered and evaporated, yielding 6.2 parts (88.3%) of 1-butyl-6-[chloro(3-chlorophenyl)methyl]-1H-benzotriazole as a residue (int. 73).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04943574
Source datasetuspto-grants-1990_07
ORD IDord-7967f0db86694135865ebc9a5fb5ede8
Source noteuspto-grants-1990_07