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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539371Generated: October 25, 2026

Water → N-(5'-Bromospiro[cyclobutane-1,2'-indene]-3'(1'H)-ylidene)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/539371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTert-ButanesulfinamideHCID 3382465—
Reactant6'-Bromospiro[cyclobutane-1,2'-inden]-1'(3'H)-oneHCID 67979616—
CatalystTitanium tetraethoxideHCID 76524—
SolventEthyl AcetateHCID 8857—
SolventHCID 178479889HCID 178479889—
ProductN-(5'-Bromospiro[cyclobutane-1,2'-indene]-3'(1'H)-ylidene)-2-methylpropane-2-sulfinamideHCID 67979440135.3%

Reaction Steps

6′-Bromospiro[cyclobutane-1,2′-inden]-1′(3′H)-one (Intermediate 38, 1.1 g, 4.38 mmol), 2-methylpropane-2-sulfinamide (0.96 g, 7.88 mmol), and titanium ethoxide (1.805 mL, 8.76 mmol) were dissolved in methyl THF (20 mL), and heated to reflux overnight. The reaction was allowed to cool to r.t., then it was diluted with EtOAc (150 mL). Water (22 mL) was added dropwise over 10 min under vigorous stirring and then the mixture was left standing without stirring for 1.5 h. The solids were filtered off and the organics were evaporated to give a crude product which was purified by flash chromatography (eluent: heptane/ethylacetate 8:1) to afford the title compound (2.1 g, 77% yield), used as such in the next step: MS (ES+) m/z 354 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865911B2
Source datasetuspto-grants-2014_10
ORD IDord-4acf26295b574b43983760287b6743fe
Source noteuspto-grants-2014_10