Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190912Generated: October 31, 2026

Hydrochloric Acid → (2-Fluoro-5-nitrophenyl)methanol

https://huagongshe.com/reaction/1190912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Fluoro-5-nitrobenzaldehydeHCID 2734770—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(2-Fluoro-5-nitrophenyl)methanolHCID 4437169—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-fluoro-5-nitro-benzaldehyde (1000 mg, 5.91 mmoles) in MeOH (10 mL) was added NaBH4 (182 mg, 4.82 mmoles). The reaction mixture was stirred for 3 h at 0° C. The reaction mixture was acidified with HCl 1M until pH4, concentrated. 50 mL of water was added and the compound was extracted with Et2O. The organic layer was dried over MgSO4, filtered, evaporated. Expected compound was obtained as a pale yellow solid (1007 mg, 99% yield). mp=62-64° C. 1H NMR (300 MHz, CDCl3) δ8.43; (dd, 6-CH, J=6.2 Hz and 2.9 Hz, 1H), 8.19; (ddd, J=9 Hz, 4.5 Hz and 2.9 Hz, 1H), 7.20; (dd, J=9.0 Hz and 9.0 Hz, 1H), 4.85; (d, J=3.6 Hz, 2H), 2.12; (s large, 1H). 13C NMR (75 MHz, CDCl3) δ125.0; (CH, d, J=10.0 Hz), 124.7; (CH, d, J=6.9 Hz), 116.2; (CH, d, J=23.6 Hz), 58.2; (CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680095B2
Source datasetuspto-grants-2014_03
ORD IDord-5fc50a1bef38428f823b5c944f2510fd
Source noteuspto-grants-2014_03