HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411310Generated: November 2, 2026
Carbon tetrabromide → 1-(2-(Trimethylsilyl)ethyl) 1'-tert-butyl 5-(bromomethyl)spiro[indoline-3,3'-pyrrolidine]-1,1'-dicarboxylate
https://huagongshe.com/reaction/1411310
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-(2-(Trimethylsilyl)ethyl) 1'-tert-butyl 5-(hydroxymethyl)spiro[indoline-3,3'-pyrrolidine]-1,1'-dicarboxylate | HCID 90449533 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-(Trimethylsilyl)ethyl) 1'-tert-butyl 5-(bromomethyl)spiro[indoline-3,3'-pyrrolidine]-1,1'-dicarboxylate | HCID 90449554 | 77.8% |
Reaction Steps
1-(2-(Trimethylsilyl)ethyl) 1′-tert-butyl 5-(hydroxymethyl)spiro[indoline-3,3′-pyrrolidine]-1,1′-dicarboxylate (441 mg, 0.98 mmol) was dissolved in methylene chloride (10 mL). Thereafter, carbon tetrabromide (359 mg, 1.08 mmol) and triphenylphosphine (310 mg, 1.18 mmol) were added to the above obtained solution under cooling on ice, and the thus obtained mixture was then stirred at the same temperature as above for 2.5 hours. Thereafter, the reaction solution was concentrated in vacuo, and the obtained residue was then purified by silica gel column chromatography (hexane:ethyl acetate=10:1) to obtain 1-(2-(trimethylsilyl)ethyl) 1′-tert-butyl 5-(bromomethyl)spiro[indoline-3,3′-pyrrolidine]-1,1′-dicarboxylate (390 mg, 77%) in the form of a colorless amorphous product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921576B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-ed837e15572a40ab8d665eb9e5b76ee4 |
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| Source note | uspto-grants-2014_12 |
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