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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Tempo | HCID 2724126 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | (2,6-Dichloro-3-fluorophenyl)methanol | HCID 67004432 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,6-Dichloro-3-fluorobenzaldehyde | HCID 18945674 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592448B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-c726c3fe37a0491eb1616882804c3306 |
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| Source note | uspto-grants-2013_11 |
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