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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873124Generated: November 2, 2026

Water → 4-Bromo-2,6-Diisopropylphenol

https://huagongshe.com/reaction/1873124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPropofolHCID 4943—
ReactantBromineHCID 24408—
SolventAcetic AcidHCID 176—
Product4-Bromo-2,6-DiisopropylphenolHCID 1042257265%

Reaction Steps

This is a modification of the procedure of Schuster, Ingeborg I.; Parvez, Masood; Freyer, Alan J. J. Org. Chem. 1988, 53, 5819. A solution of bromine (6.3 mL, 119 mmol) in acetic acid (40 mL) was added dropwise to a stirred, room temperature solution of 2,6-diisopropylphenol (20 mL, 97.1 mmol of 90% tech. grade) in acetic acid (280 mL). After 6 h, water was added and the mixture was extracted with ether. The ether phase was dried and concentrated and the residue was flash chromatographed (petroleum ether: eluent) to provide 4-bromo-2,6-diisopropylphenol (16.2 g, 65%) as a red oil. This oil was dissolved in DMF (50 mL), iodomethane (11.7 mL, 189 mmol) and potassium carbonate (26.3 g, 117 mL) were added to it. This reaction mixture was stirred for 5 h and diluted with water. This mixture was extracted with ether and the ether extracts were dried, concentrated and flash chromatographed (petroleum ether: eluent) to provide the title compound as a colorless oil (15.4 g, 90%): NMR (CDCl3); δ 7.17 (s, 2H), 3.70 (s, 3H), 3.29 (septet, 1H), 1.20 (d, 12 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06110962
Source datasetuspto-grants-2000_08
ORD IDord-3c38f0d8aa3545bb89053cddd1f65b1a
Source noteuspto-grants-2000_08