Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573717Generated: October 31, 2026

Tetrahydrofuran → (S)-((S)-5'-(tert-butyldimethylsilyloxy)-4'-iodo-2'-isopropyl-6',8'-dihydro-5'H-spiro[cyclobutane-1,7'-quinoline]-3-yl)(4-(pentafluorosulfanyl)phenyl)methanol

https://huagongshe.com/reaction/573717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-Iodophenylsulfur PentafluorideHCID 2779199—
Reactant(S)-5'-(tert-butyldimethylsilyloxy)-4'-iodo-2'-isopropyl-6',8'-dihydro-5'H-spiro[cyclobutane-1,7'-quinoline]-3'-carbaldehydeHCID 86662517—
ReactantHCID 178418918HCID 178418918—
ReactantHCID 178461733HCID 178461733—
Product(S)-((S)-5'-(tert-butyldimethylsilyloxy)-4'-iodo-2'-isopropyl-6',8'-dihydro-5'H-spiro[cyclobutane-1,7'-quinoline]-3-yl)(4-(pentafluorosulfanyl)phenyl)methanolHCID 86662516—

Reaction Steps

Obtained by starting from (S)-5′-(tert-butyldimethylsilyloxy)-4′-iodo-2′-isopropyl-6′,8′-dihydro-5′H-spiro[cyclobutane-1,7′-quinoline]-3′-carbaldehyde and 1-iodo-4-pentafluorosulfanyl-benzene. A 1.3 M solution of isopropylmagnesium chloride-lithium chloride-complex in tetrahydrofurane is used instead of a 2 M solution of isopropylmagnesium chloride in tetrahydrofurane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029544B2
Source datasetuspto-grants-2015_05
ORD IDord-2de8249dcc7e49b1aa3bc5ae09f298d7
Source noteuspto-grants-2015_05