Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096664Generated: October 31, 2026

Cyclohexanone → HCID 66718361, compound

https://huagongshe.com/reaction/2096664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantPyridine, 2-bromo-6-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-HCID 11483477—
ProductHCID 66718361HCID 6671836115%

Reaction Steps

Prepared from 6-bromo-O-(tert-butyldimethylsilyl)-2-pyridinemethanol and cyclohexanone by the method described in Example 10 to give the title compound (0.49 g, 15%) as a yellow oil; NMR δH (400 MHz, CDCl3) 0.13 (6H, s), 0.96 (9H, s), 1.61-1.91 (10H, m), 4.82 (2H, s), 5.17 (1H, s), 7.21 (1H, dd, J 8.0 Hz, 1.0 Hz), 7.38 (1H, dd, J 7.5 Hz), 1.0 Hz), 7.71 (1H, t, J 7.5 Hz). TLC (Hex:EtOAc (9:1)) Rf=0.30**

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450328B2
Source datasetuspto-grants-2013_05
ORD IDord-150436c2f2a1404ca24f74b4ee0f47b7
Source noteuspto-grants-2013_05