HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377132Generated: October 26, 2026
Hexane → (3-ethoxy-4-methoxy-phenyl)-(1-methyl-1H-benzotriazol-5-yl)-methanol
https://huagongshe.com/reaction/2377132
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexane | HCID 8058 | — |
| Reactant | 1-methyl-1H-1,2,3-benzotriazole-5-carbaldehyde | HCID 2795417 | — |
| Reactant | 4-Bromo-2-ethoxy-1-methoxybenzene | HCID 21772690 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-ethoxy-4-methoxy-phenyl)-(1-methyl-1H-benzotriazol-5-yl)-methanol | HCID 68939793 | 106.4% |
Reaction Steps
To a solution of 4-bromo-2-ethoxy-1-methoxy-benzene (1.5 g, 6.5 mmol) in THF (15 mL) was added a solution of n-butyllitium in hexane (2.5 mL, 2.5 N, 6.3 mmol) at −78° C. and kept for 20 min. To the mixture was added a slurry of 1-methyl-1H-benzotriazole-5-carbaldehyde (1.0 g, 6.0 mmol) in THF (5 mL) at −78° C. After 18 h, isopropanol (2 mL) and water (10 mL) was added to the mixture, and the cold bath was removed. The mixture was stirred at room temperature for 20 min. The mixture was extracted with ethyl acetate (50 mL) and water (50 mL). The aqueous layer was extracted with ethyl acetate (50 mL). The combined organic layers was washed with water (50 mL), brine (50 mL) and dried over MgSO4. Removal of solvent gave (3-ethoxy-4-methoxy-phenyl)-(1-methyl-1H-benzotriazol-5-yl)-methanol as an oil (2 g). The oil was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468446B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-8aec90f965a646ae91c6322b0303dde2 |
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| Source note | uspto-grants-2008_12 |
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