HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432899Generated: November 1, 2026
Methanamine, N-methoxy-, hydrochloride (1:1) → HCID 54064141, compound
https://huagongshe.com/reaction/1432899
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | HCID 13273790 | HCID 13273790 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54064141 | HCID 54064141 | 78.5% |
Reaction Steps
N,N-Dimethylaminopyridine (2.60 g, 21.3 mmol) and BOP reagent (18.15 g, 41.0 mmol) are added to a solution of 2-tert-butoxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-propionic acid (12.37 g, 38.7 mmol), diisopropylethylamine (8.1 mL, 46.4 mmol) and N,O-dimethylhydroxylamine hydrochloride (4.53 g, 46.4 mmol) in THF (260 mL) at RT. The resulting suspension is stirred at RT overnight then concentrated to dryness. The residue is diluted with EtOAc and washed with saturated NH4Cl, saturated NaHCO3 and brine. The organic layer is dried over MgSO4, filtered and concentrated in vacuo to give the crude product which is purified by flash chromatography eluting with 10-30% EtOAc/Hexanes to yield the title compound (11.86 g, 30.37 mmol) as an oil. 1H NMR (CDCl3, 300 MHz) δ5.35 (bd, 1H), 4.71 (bs, 1H), 3.78-3.85 (m, 2H), 3.72 (s, 3H), 3.20 (s, 3H), 1.42 (s, 9H), 0.90 (s, 9H), 0.05 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612075B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-849cd6e6c1f0478182bf2bb01cfa655b |
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| Source note | uspto-grants-2009_11 |
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