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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170758Generated: October 25, 2026

Ammonium Chloride → (2-Chloro-5-nitro-phenyl)-(4-chloro-phenyl)-methanol

https://huagongshe.com/reaction/2170758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Chloro-5-nitrobenzaldehydeHCID 72933—
ReactantAcetone cardiceHCID 18522661—
ReactantHCID 178478191HCID 178478191—
SolventTetrahydrofuranHCID 8028—
Product(2-Chloro-5-nitro-phenyl)-(4-chloro-phenyl)-methanolHCID 5843815690%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of (4-chlorophenyl)magnesium bromide (1M in Et2O, 81 ml, 81 mmol) in THF (200 ml) was added drop wise a solution of 2-chloro-5-nitrobenzaldehyde (10 g, 53.9 mmol) in THF (100 ml) at −78° C. (dry ice/acetone bath). After the addition, the reaction mixture was further stirred at −78° C. for 1 h then 10 min at 0° C. (ice bath). A saturated aqueous NH4Cl solution (400 ml) was added and the resulting mixture was extracted with AcOEt (2×400 ml). The combined organic layers were washed with brine then dried over Na2SO4, filtered and evaporated to dryness. The resulting crude material was purified by Combi-Flash Companion™ (Isco Inc.) column chromatography (SiO2; gradient elution, heptane/TBME 95:5→6:4) to yield the title compound (14.4 g, 48.4 mmol, 90%) as a beige solid. TLC: RF=0.80 (heptane/DCM/TBME 1:1:2); HPLC: AtRet=2.43 min; LC-MS: m/z not detected; 1H NMR (400 MHz, CDCl3): 6.20 (s, 1H), 7.36 (s, 4H), 7.53 (d, J=8.6, 1H), 8.13 (dd, J=8.8, 2.9, 1H), 8.66 (d, J=2.7, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051279B2
Source datasetuspto-grants-2015_06
ORD IDord-8a3866298ff84d66ab5a94f82ca80cea
Source noteuspto-grants-2015_06