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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720768Generated: October 30, 2026

Hydrochloric Acid → HCID 178490127, compound

https://huagongshe.com/reaction/720768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantMagnesiumHCID 5462224—
Reactant5-Bromo-1,3-di-tert-butyl-2-methoxybenzeneHCID 13691541—
ReactantDimethylphosphiteHCID 21884954—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178490127HCID 17849012727.2%

Reaction Conditions

Temperature5 °C

Reaction Steps

Under argon atmosphere, a solution of magnesium (4.0 g, 0.95 equivalents) and a small amount of iodine in THF (50 mL) was stirred at room temperature for 1 hour. After 4-bromo-2,6-di-tert-butylanisole (52 g, 0.175 mol) synthesized in Reference Example 2 was added at 46° C. to 53° C. thereto, the mixture was stirred at 5° C. for 1 hour. Then, dimethyl phosphite (11.4 g, 0.52 equivalents) was added and the mixture was stirred at 5° C. for 1 hour. After water (50 mL) was added at 3° C. and toluene (50 mL) and 6M-HCl (20 mL) were then added, the mixture was stirred at room temperature for 30 minutes. The reaction solution was allowed to separate into layers. An organic layer was washed successively with water (20 mL), a 5% NaHCO3 aqueous solution (20 mL) and a 5% NaCl aqueous solution (20 mL), dried over anhydrous magnesium sulfate and then naturally filtered. The filtrate was concentrated under reduced pressure. The residue was recrystallized from heptane to obtain the title compound (11.6 g, pale yellowish white crystal). Yield 20.5%, mp. 166.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135582B2
Source datasetuspto-grants-2006_11
ORD IDord-ac34e7535139423385828f0f73ee2ea8
Source noteuspto-grants-2006_11