HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602824Generated: October 31, 2026
Trimethyl orthoformate → HCID 57948569, compound
https://huagongshe.com/reaction/602824
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-azetidinecarboxylic Acid | HCID 93192 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Reactant | HCID 86635605 | HCID 86635605 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57948569 | HCID 57948569 | 62.7% |
Reaction Steps
Azetidine-3-carboxylic acid (46 mg) and sodium hydroxide (18 mg) were dissolved in methanol (4 mL). To this solution, trimethoxymethane (0.050 mL) and a tetrahydrofuran (1 mL)-methanol (1 mL) mixed solution of 6-[3-(4-chlorophenyl)propoxy]-3,4-dihydronaphthalene-2-carboaldehyde (100 mg) were successively added under ice cooling. The reaction mixture was stirred for 3.5 hours under ice cooling. To the reaction mixture, sodium borohydride (17 mg) was added under ice cooling. The reaction mixture was stirred under ice cooling for 20 minutes. Thereafter, 4 mol/L hydrogen chloride/ethyl acetate solution was added until it was neutral, and concentrated. The obtained residue was purified by flash silica gel column chromatography (chloroform:methanol:aqueous ammonia=80:10:1 to 80:20:4), to thereby obtain the title compound (79 mg) having the following physical properties.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07906549B2 |
|---|
| Source dataset | uspto-grants-2011_03 |
|---|
| ORD ID | ord-288b3d231a7c42c6ad0d3e8a46d329fb |
|---|
| Source note | uspto-grants-2011_03 |
|---|