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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624002Generated: October 27, 2026

Iodine → 2-Amino-2-isopropylpropane-1,3-diol

https://huagongshe.com/reaction/1624002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantMethanolHCID 887—
Reactant2-Amino-2-(hydroxymethyl)-3-methylbutanoic acidHCID 2733898—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product2-Amino-2-isopropylpropane-1,3-diolHCID 1233927111.3%

Reaction Conditions

Temperature66 °C

Reaction Steps

To a solution of 2-amino-2-(hydroxymethyl)-3-methylbutanoic acid (2943 mg, 20 mmol) in THF (60 mL) was added sodium borohydride (2270 mg, 60.0 mmol). The reaction was cooled in an ice bath, and a THF (10 mL) solution of iodine (7614 mg, 30.0 mmol) was added dropwise. The mixture was refluxed (66° C.) for 16 h. The reaction was cooled in an ice bath, and methanol (10 mL) was added (dropwise at first) followed by brine (75 mL). The mixture was extracted with ethyl acetate (2×50 mL). The combined organic extracts were washed with brine, dried (MgSO4), then filtered. 4 M HCl in dioxane (6 mL) was added. The mixture was then concentrated. Ether was added, and the precipitate was collected to give the title compound (300 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778950B2
Source datasetuspto-grants-2014_07
ORD IDord-609317fef5d84d8db8dd71447c018295
Source noteuspto-grants-2014_07