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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155342Generated: October 30, 2026

Hydrogen Bromide → 3-Hydroxy-4,5,6,7-tetrahydroisoxazolo[5,4-c]pyridinium bromide

https://huagongshe.com/reaction/1155342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantMethanolHCID 887—
ReactantPotassium BromideHCID 253877—
ReactantHCID 178501908HCID 178501908—
SolventAcetic AcidHCID 176—
Product3-Hydroxy-4,5,6,7-tetrahydroisoxazolo[5,4-c]pyridinium bromideHCID 70082568—

Reaction Steps

A solution of methyl 3-hydroxy-4,5,6,7-tetrahydroisoxazolo[5, 4-c]-pyridine-6-carboxylate (309 mg; 1.6 mmol) in a solution of hydrogen bromide in glacial acetic acid (3 ml; 43%) was refluxed for 15 minutes. Upon evaporation to dryness in vacuo the residue was treated with the same reagent (3 ml) for further 15 minutes. Evaporation of the reaction mixture to dryness in vacuo and recrystallization (methanol-ether) of the residue gave Ia (salt) (193 mg; 56%) as faintly reddish crystals, m.p. 162-163° C. (decomp.). IR (KBr): 3700-3300 (m), 3070 (s), 3000-2300 (several bands, m-s), 1670 (m), 1580 (m), 1525 (s), 1505 (w) cm-1. UV (methanol): <210 nm. 1H NMR [D2O (sodium 3-(trimethylsilyl) propanesulfonate was used as an internal standard)]: δ4.77 (ca. 5 H, s), 4.43 (2 H, t, J 1 Hz), 3.7- 3.4 (2 H, q, J 6 and 7 Hz), 3.0-2.7 (2 H, t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04301287
Source datasetuspto-grants-1981_11
ORD IDord-eaa2bb7851074f4cb58f61a46e6f16fd
Source noteuspto-grants-1981_11