HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715729Generated: November 4, 2026
Isobutyl nitrite → (R)-6-Benzyloxy-1-(2-hydroxypropyl)indazole
https://huagongshe.com/reaction/1715729
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutyl nitrite | HCID 10958 | — |
| Reactant | Phosphinic Acid | HCID 4124402 | — |
| Reactant | (R)-6-Benzyloxy-1-(2-hydroxypropyl)-3-aminoindazole | HCID 11635595 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | (R)-6-Benzyloxy-1-(2-hydroxypropyl)indazole | HCID 11587260 | — |
Reaction Steps
Hypophosphorous acid (3.45 L of a 50% (w/w) aqueous solution) was added to a stirred solution of 2 (1975 g, 6.65 mol) in 23.7 L of methanol under a nitrogen atmosphere. Isobutyl nitrite (1576 mL, 13.3 mol) was added in two portions, keeping the reaction temperature below 53° C. After 3 hours, a solution of Na2HPO4 (8.5 kg) in 70 L of water was added, and the mixture was extracted with ethyl acetate (30 L then 15 L). The combined organic extracts were washed with brine, dried (Na2SO4), treated with decolorizing charcoal, filtered and concentrated in vacuo. The product was purified by trituration with ethyl acetate-hexane followed by elution through silica using an acetone-hexane gradient, to give after concentration in vacuo, 1260 g (67%) of 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07799930B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-859eade6e647493b9b7663af95578ffc |
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| Source note | uspto-grants-2010_09 |
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