HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257525Generated: November 2, 2026
Sodium Thiosulfate Pentahydrate → Tert-butyl 3-bromo-5-formylbenzoate
https://huagongshe.com/reaction/1257525
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate Pentahydrate | HCID 61475 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | Tempo | HCID 2724126 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | Tert-butyl 3-bromo-5-(hydroxymethyl)benzoate | HCID 58096191 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | Tert-butyl 3-bromo-5-formylbenzoate | HCID 58095966 | — |
Reaction Steps
To a suspension of potassium bromide (249.3 g, 2.095 mol), 2,2,6,6-tetramethylpiperidine 1-oxyl (3.27 g, 20.93 mmol) in saturated aqueous sodium bicarbonate (960 mL) and water (240 mL) were added tert-butyl 3-bromo-5-(hydroxymethyl)benzoate (119.7 g, 417 mmol) and dichloromethane (1200 mL). The mixture was cooled to <5° C. and sodium hypochlorite (850 mL, 12.53 mol) was added dropwise in 4 portions until the reaction completed. A solution of sodium thiosulfate pentahydrate (72 g) in water (250 mL) was added and the reaction mixture was warmed to ambient temperature. The organic layer was separated and the aqueous layer was extracted with dichloromethane (2×). The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated (119.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461185B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-d48244ab4a1e49c7bf7736ebdd649576 |
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| Source note | uspto-grants-2013_06 |
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