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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411286Generated: October 31, 2026

Sodium Thiosulfate → HCID 90449581, compound

https://huagongshe.com/reaction/1411286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 90449612HCID 90449612—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
ProductHCID 90449581HCID 9044958171%

Reaction Conditions

Temperature60 °C

Reaction Steps

1-(2-(Trimethylsilyl)ethyl) 1′-tert-butyl spiro[indoline-3,3′-pyrrolidine]-1,1′-dicarboxylate (15.2 g, 36.5 mmol) was dissolved in t-butanol (240 mL) and water (40 mL). Thereafter, N-bromosuccinimide (7.9 g, 44.4 mmol) was added to the above obtained solution at room temperature, and the thus obtained mixture was then stirred at 60° C. for 15 hours. Thereafter, an aqueous solution of sodium thiosulfate was added to the reaction solution, and the mixed solution was then extracted with ethyl acetate. The organic layer was washed with brine, and was then dried over anhydrous sodium sulfate, followed by concentration in vacuo. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=3:1) to obtain 1-(2-(trimethylsilyl)ethyl) 1′-tert-butyl 5-bromospiro[indoline-3,3′-pyrrolidine]-1,1′-dicarboxylate (12.9 g, 71%) in the form of a white amorphous product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921576B2
Source datasetuspto-grants-2014_12
ORD IDord-635cbadfdb304faa9593691696b2a282
Source noteuspto-grants-2014_12