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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406271Generated: October 29, 2026

tert-Butylsulfinamide, (R)-(+)- → HCID 89612070, compound

https://huagongshe.com/reaction/2406271

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butylsulfinamide, (R)-(+)-HCID 10964479—
ReactantHCID 86686865HCID 86686865—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89612070HCID 8961207050%

Reaction Conditions

Temperature68 °C

Reaction Steps

A 22 L multi-neck reactor equipped with a condenser, a nitrogen inlet, a heating mantle and an overhead mechanical stirrer was charged with 5-chloro-2-methoxy-2,3-dihydro-1H-inden-1-one (18) (622.88 g, 3.17 mol) and (R)-tert-butylsulfinamide (460.7 g, 3.8 mol). Tetrahydrofuran (3100 mL) was added to the mixture and the temperature dropped to 9° C. Ti(OEt)4 (985 mL, 4.76 mol) was added over 10 minutes. The mixture was heated to 68° C. and all solids dissolved at about 35° C. After 5 hours, the reaction achieved a 50% yield as determined by HPLC wt % assay. The reaction was stirred at 68° C. for an additional 5 hours until the undesired diastereomer decomposed to less than 5% (AUC). The reaction was cooled to ambient temperature over 2 hours and stirred for 16 hours. HPLC analysis indicated no obvious change in reaction profile during this period. This crude reaction mixture was taken in to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809356B2
Source datasetuspto-grants-2014_08
ORD IDord-7deb9bc99fdd4d1f85e2e19a0d01bc49
Source noteuspto-grants-2014_08