HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158466Generated: October 26, 2026
5-Bromo-2-methoxybenzaldehyde → 5-Bromo-2-methoxybenzyl alcohol
https://huagongshe.com/reaction/1158466
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Bromo-2-methoxybenzaldehyde | HCID 90684 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Bromo-2-methoxybenzyl alcohol | HCID 612298 | — |
Reaction Steps
To a suspension of 5-bromo-2-methoxy-benzaldehyde (7.00 g, 32.2 mmol) in MeOH (40 mL), cooled to 0 to 5° C., is added NaBH4 (1.40 g, 35.4 mmol). After stirring for 1 h, the mixture is poured into ice-water, followed by extraction with AcOEt. The combined organics are washed with brine, dried (Na2SO4) and concentrated to give the title product as off-white solid. TLC, Rf (hexane/AcOEt 3:1)=0.19. 1H-NMR (CDCl3): δ 2.24 (m, 2H), 3.88 (s, 3H), 4.68 (d, 2H), 6.79 (dd, 1H), 7.41 (dd, 1H), 7.45 (d, 1H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07807709B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-071f0d3d70da4e82a2a27309cf0553e0 |
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| Source note | uspto-grants-2010_10 |
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