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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858704Generated: October 30, 2026

Sodium borohydride → HCID 58762592, compound

https://huagongshe.com/reaction/858704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-broMo-2-fluoro-5-Methoxy-benzaldehydeHCID 57527288—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 58762592HCID 58762592—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-Bromo-2-fluoro-5-methoxy-benzaldehyde (4.03 g, 17.33 mmol) from step (1) below in Methanol at 0° C. was added NaBH4 (0.65 g, 17.33 mmol). After the reaction mixture was stirred at 0° C. for 2 hours, it was allowed to warm to room temperature. The organic layer was taken up in ethyl ether, washed with water and dried over MgSO4, filtered and concentrated. The residue was purified by flash chromatography (25–45% EtOAc in hexanes) to give the product. Yield: 3.90 g, 99.0%. 1H NMR (CDCl3) δ: 3.90 (s, 3H), 4.74 (d, J=6.02 Hz, 2H), 6.82 (d, J=6.1 Hz, 1H), 7.29 (d, J=10.58 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148226B2
Source datasetuspto-grants-2006_12
ORD IDord-0631f7cff48c4904950a90e079715060
Source noteuspto-grants-2006_12