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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046911Generated: October 25, 2026

Sodium Bromide → 2,6-Dichloro-3-fluorobenzaldehyde

https://huagongshe.com/reaction/2046911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BromideHCID 253881—
ReactantSodium BicarbonateHCID 516892—
ReactantTempoHCID 2724126—
ReactantSodium HypochloriteHCID 23665760—
Reactant(2,6-Dichloro-3-fluorophenyl)methanolHCID 67004432—
SolventDichloromethaneHCID 6344—
Product2,6-Dichloro-3-fluorobenzaldehydeHCID 18945674—

Reaction Conditions

Temperature-7 °C

Reaction Steps

To a solution of (2,6-Dichloro-3-fluorophenyl)methanol (100 g, 0.51 mol) in dichloromethane (450 mL) was added a solution of sodium bromide (54 g, 0.53 mol, in 90 mL water). The rapidly stirred biphasic mixture was cooled to −7° C. and TEMPO (1.54 g, 0.0100 mol) was added. A solution of 0.81M sodium hypochlorite (823 mL, 0.66 mol) saturated with sodium bicarbonate (75 g) was added dropwise over a period of 1 h while maintaining the temperature below −2° C. After the addition the reaction mixture was stirred for 30 min. The two layers separated and the DCM layer was washed with aq. solution of sodium thiosulfate. The DCM layer was dried (Na2SO4) and concentrated on rotary evaporator without using vacuum (aldehyde is volatile) to give the title compound as a solid, mp. 63-65° C. 1H NMR (CDCl3, 300 MHz): δ=7.23 (dd, 1H, J=7.8, 9.0 Hz), 7.35 (dd, 1H, J=4.5, 9.3 Hz), 10.2 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592448B2
Source datasetuspto-grants-2013_11
ORD IDord-c726c3fe37a0491eb1616882804c3306
Source noteuspto-grants-2013_11