HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507942Generated: November 4, 2026
Methanol → (4-Isobutoxy-3-{[(2-phenylethyl)(4-phenyl-1,3-thiazol-2-yl)amino]methyl}phenyl)methanol
https://huagongshe.com/reaction/507942
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Isobutoxy-3-{[(2-phenylethyl)(4-phenyl-1,3-thiazol-2-yl)amino]methyl}benzaldehyde | HCID 23157491 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (4-Isobutoxy-3-{[(2-phenylethyl)(4-phenyl-1,3-thiazol-2-yl)amino]methyl}phenyl)methanol | HCID 23157600 | 89.1% |
Reaction Steps
To a mixture of 4-isobutoxy-3-{[(2-phenylethyl)(4-phenyl-1,3-thiazol-2-yl)amino]methyl}benzaldehyde (1.43 g, 3.04 mmol), methanol (5 mL) and tetrahydrofuran (10 mL) was added sodium borohydride (58 mg, 1.52 mmol) under stirring at 0° C., and the mixture was stirred at the same temperature for 2 hr. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1-1/1) to give the title compound (1.28 g, yield 88%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786165B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-c46fe404ed2e4fe48f0e7a742ced5b54 |
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| Source note | uspto-grants-2010_08 |
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