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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2-Amino-2-(hydroxymethyl)-3-methylbutanoic acid | HCID 2733898 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-Amino-2-isopropylpropane-1,3-diol | HCID 12339271 | 11.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08778950B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-609317fef5d84d8db8dd71447c018295 |
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| Source note | uspto-grants-2014_07 |
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