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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578632Generated: November 1, 2026

Hydrogen Bromide → Terbutaline

https://huagongshe.com/reaction/1578632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
ReactantHCID 21450028HCID 21450028—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductTerbutalineHCID 5403—

Reaction Steps

1.1 g of this salt were dissolved in warm absolute ethanol and 0.1 g 10% palladium charcoal were added. The solution was then hydrogenated at 50°C. and 5 atmospheres pressure overnight. The catalyst was filtered off and the volume of the solution reduced by evaporation. The hydrobromide of 1-(3',5'-diacetoxyphenyl)-2-(t-butylamino)-ethanol with 1 mole of water was precipitated by the addition of ether. M.p. 108°-111°C. The protective acetyl groups may be removed by boiling the 1-(3',5'-diacetoxyphenyl)-2-(t-butylamino)-ethanol hydrobromide with 1% hydrobromic acid for three hours. After evaporation and drying the product was recrystallized as described in Example 2c.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03937838
Source datasetuspto-grants-1976_02
ORD IDord-4bf788f4a52546c5a3c6af9d21f00452
Source noteuspto-grants-1976_02