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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010545Generated: October 25, 2026

Sulfuric acid magnesium salt (1:1) → (tert-butoxy)-N-(2-{[(4-methoxyphenyl)methyl](oxolan-3-ylmethyl)amino}ethyl)carboxamide

https://huagongshe.com/reaction/1010545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant3-Furancarboxaldehyde, tetrahydro-HCID 157568—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantTert-butyl N-(2-{[(4-methoxyphenyl)methyl]amino}ethyl)carbamateHCID 112688707—
Solvent1,2-DichloroethaneHCID 11—
Product(tert-butoxy)-N-(2-{[(4-methoxyphenyl)methyl](oxolan-3-ylmethyl)amino}ethyl)carboxamideHCID 13172899780.9%

Reaction Steps

This compound was made in a manner analogous to that set forth in Step D of Example 5, using 0.2 gram (0.0020 mole) of (oxolan-3-yl)formaldehyde, 0.56 gram (0.0020 mole) of (tert-butoxy)-N-(2-{[(4-methoxyphenyl)methyl]amino}-ethyl)carboxamide (prepared in Step A of Example 9), 0.64 gram (0.0030 mole) of sodium triacetoxyborohydride and 2.5 grams (0.021 mole) of magnesium sulfate in 50 mL of 1,2-dichloroethane. The reaction product was purified with column chromatography on silica gel. Elution was accomplished using a mixture of 1% methanol in methylene chloride as an eluant. Appropriate fractions were combined and concentrated under reduced pressure, yielding 0.59 gram of the subject compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977332B2
Source datasetuspto-grants-2011_07
ORD IDord-ab9d4328df8b41dcbeb9a02578764ec8
Source noteuspto-grants-2011_07