HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720768Generated: October 30, 2026
Hydrochloric Acid → HCID 178490127, compound
https://huagongshe.com/reaction/720768
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 5-Bromo-1,3-di-tert-butyl-2-methoxybenzene | HCID 13691541 | — |
| Reactant | Dimethylphosphite | HCID 21884954 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178490127 | HCID 178490127 | 27.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07135582B2 |
|---|
| Source dataset | uspto-grants-2006_11 |
|---|
| ORD ID | ord-ac34e7535139423385828f0f73ee2ea8 |
|---|
| Source note | uspto-grants-2006_11 |
|---|