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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium Thiosulfate PentahydrateHCID 61475—
ReactantPotassium BromideHCID 253877—
ReactantTempoHCID 2724126—
ReactantSodium HypochloriteHCID 23665760—
ReactantTert-butyl 3-bromo-5-(hydroxymethyl)benzoateHCID 58096191—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductTert-butyl 3-bromo-5-formylbenzoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461185B2
Source datasetuspto-grants-2013_06
ORD IDord-d48244ab4a1e49c7bf7736ebdd649576
Source noteuspto-grants-2013_06