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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695259Generated: October 30, 2026

2-Chloro-6-methylphenol → HCID 67246220, compound

https://huagongshe.com/reaction/1695259

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-methylphenolHCID 6898—
ReactantTriethylamineHCID 8471—
ReactantN-bromobutanimideHCID 67184—
Reactanttert-ButyldimethylsilaneHCID 5072427—
ReactantHCID 57999891HCID 57999891—
ReactantHCID 67246834HCID 67246834—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 67246220HCID 67246220—

Reaction Conditions

Temperature25 °C

Reaction Steps

Triethyl amine (36 mL, 0.263 mol) was added to a solution of (2-bromomethyl-6-chloro-phenoxy)-tert-butyl-dimethyl-silane (72 g, 0.214 mol) [prepared from 6-chloro cresol by protecting the hydroxy group with t-butyldimethylsilane followed by bromination using N-bromosuccinimide] and compound of Example 1f (43 g, 0.164 mol) in chloroform (600 mL) at 5° C. over a period of 20 min. The reaction mixture was stirred at 25° C. for 30 min. The reaction mixture was washed with water (2×200 mL) and brine (100 mL). The solvent was removed under reduced pressure and to the oily mass obtained, methanol (300 mL) was added with stirring. The crystalline solid obtained was filtered, washed with methanol and dried to obtain the title compound. Yield: 70 g, (83%); 1H NMR (CDCl3, 300 MHz): δ 0.28 (s, 6H, 2CH3), 1.03 (s, 9H, 3CH3), 2.45 (s, 3H, CH3), 3.89 (s, 3H, OCH3), 4.19 (s, 2H, CH2), 6.89 (t, 1H, Ar), 7.24 (t, 1H, Ar), 7.32 (d, 1H, Ar), 7.61 (s, 1H, Ar), 7.69 (s, 1H, Ar); MS: m/e (ES−) 515 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163730B2
Source datasetuspto-grants-2012_04
ORD IDord-7165219f102648d2b5621f1737dc1d82
Source noteuspto-grants-2012_04