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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394639Generated: October 30, 2026

HCID 17952680, compound → HCID 17952821, compound

https://huagongshe.com/reaction/1394639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 17952680HCID 17952680—
ReactantHCID 178418287HCID 178418287—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 17952821HCID 1795282194%

Reaction Steps

(5-Bromo-2-fluoro-phenyl)-(2-ethoxy-3,5-diisopropyl-phenyl)-methanol (1.88 g, 4.6 mmol) was dissolved in dichloromethane (5 ml) and added to a suspension of pyridinium chlorochromate (1.1 g, 5.1 mmol) in dichloromethane (20 ml). After stirring at ambient temperature under and atmosphere of nitrogen for 4 h the reaction was diluted with ether (50 mL) and filtered through a plug of florosil. The remaining solvent was evaporated to yield (5-bromo-2-fluoro-phenyl)-(2-ethoxy-3,5-diisopropyl-phenyl)-methanone as yellow crystals (1.75 g, 94%). 1H NMR (250 MHz, CDCl3): δ 7.81 (dd, 1H, J=3.1, J=6.9), 7.62 (m, 1H), 7.33 (d, 1H, J=2.5), 7.28 (d, 1H, J=2.5), 7.02 (dd, 1H, J=11.2, J=9.4), 3.67 (q, 2H, J=6.9), 3.34 (m, 1H), 2.95 (m, 1H), 1.31 (s, 3H), 1.28 (s, 6H), 1.25 (s, 3H), 1.02 (t, 3H, J=6.9). MS [EI+] 407, 409 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348359B2
Source datasetuspto-grants-2008_03
ORD IDord-275cc3f2a72b4d628ee11d88f527c7dd
Source noteuspto-grants-2008_03