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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097285Generated: October 30, 2026

3-Nitrobenzaldehyde → 3-Nitrobenzyl alcohol

https://huagongshe.com/reaction/1097285

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrobenzaldehydeHCID 7449—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product3-Nitrobenzyl alcoholHCID 6926798.6%

Reaction Steps

To a solution of 3-nitrobenzaldehyde (5 g, 33.1 mmol) in MeOH (25 mL) at ambient temperature was added NaBH4 (1.25 g, 33.1 mmol) and the resulting mixture was stirred for 30 min. The reaction mixture was quenched with water. The product was extracted with CH2Cl2 thrice and the combined organic extracts were washed with H2O followed by brine, dried over Na2SO4 and concentrated under reduced pressure to furnish without purification 5 g of compound (xB). 1H NMR (CDCl3): δ 8.27 (s, 1H), 8.17 (dd, 1H), 7.73 (dd, 1H), 7.57 (t, 1H), 4.85 (s, 2H), 2.07 (s, 1H). MS (m/z): 154 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143255B2
Source datasetuspto-grants-2012_03
ORD IDord-f2a90fe267f14db49362de6d7f50bbfd
Source noteuspto-grants-2012_03