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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644403Generated: October 30, 2026

Hydrochloric Acid → 5-(1,1-Dimethylethyl)salicylic acid

https://huagongshe.com/reaction/644403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfamic AcidHCID 5987—
ReactantSodium SulfiteHCID 24437—
Reactant5-tert-ButylsalicylaldehydeHCID 1475090—
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product5-(1,1-Dimethylethyl)salicylic acidHCID 8528177.4%

Reaction Steps

Sulfamic acid (1.76 g, 18.1 mmol) and sodium dihydrogenphosphate (7.33 g, 47 mmol) were added to a solution of 5-[(1,1-dimethyl)ethyl]-2-hydroxybenzaldehyde (2.15 g, 12.1 mmol) in 1,4-dioxane (100 mL) and water (40 mL). A solution of sodium chlorite (1.76 g, 15.5 mmol) in water (10 mL) was added to the mixture under ice cooling, and it was stirred for 1 hour. Then, sodium sulfite (1.80 g, 14.3 mmol) was added to the mixture, and it was stirred for 30 minutes. Concentrated hydrochloric acid was added to the reaction mixture, and pH was adjusted to 1. The residue obtained by evaporation of 1,4-dioxane under reduced pressure was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was washed with n-hexane under suspension to give the title compound (1.81 g, 77.4%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700655B2
Source datasetuspto-grants-2010_04
ORD IDord-2264af9ccfcd423fa411b486b2d2147d
Source noteuspto-grants-2010_04