HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629423Generated: October 30, 2026
Sulfuric acid magnesium salt (1:1) → 1,5-anhydro-2,4-dideoxy-2-(6-(4-methoxybenzyl)-4,5-dimethyl-1-oxo-1,3-dihydro-2H-isoindol-2-yl)-L-threo-pentitol
https://huagongshe.com/reaction/629423
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | (3S,4S)-3-Aminotetrahydro-2H-pyran-4-OL | HCID 55285677 | — |
| Reactant | Methyl 2-formyl-5-(4-methoxybenzyl)-3,4-dimethylbenzoate | HCID 118468425 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,5-anhydro-2,4-dideoxy-2-(6-(4-methoxybenzyl)-4,5-dimethyl-1-oxo-1,3-dihydro-2H-isoindol-2-yl)-L-threo-pentitol | HCID 118468151 | 32.8% |
Reaction Steps
To a solution of methyl 2-formyl-5-(4-methoxybenzyl)-3,4-dimethylbenzoate (0.10 g) in THF (1.90 mL) were added (3S,4S)-3-aminotetrahydro-2H-pyran-4-ol (0.04 g) and anhydrous magnesium sulfate (0.07 g), and the mixture was stirred at room temperature for 5 hr. The insoluble substance was removed by filtration, and the filtrate was concentrated. The residue was diluted with methanol (1.90 mL)-THF (1.90 mL), sodium triacetoxyborohydride (0.13 g) was added thereto, and the mixture was stirred at room temperature for 2.5 days. The reaction mixture was diluted with ethyl acetate, and the mixture was washed with water and saturated brine. The organic layer was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (0.04 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09315458B2 |
|---|
| Source dataset | uspto-grants-2016_04 |
|---|
| ORD ID | ord-f9a1b7dc14d4476fa5f6a66b9371f166 |
|---|
| Source note | uspto-grants-2016_04 |
|---|