HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830209Generated: November 1, 2026
Ammonium Chloride → 1-(3,4,5,6-Tetramethoxy-2-methylphenyl)-1-(3-benzyloxyphenyl)methanol
https://huagongshe.com/reaction/1830209
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-(Benzyloxy)-3-bromobenzene | HCID 2756638 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2,3,4,5-Tetramethoxy-6-methylbenzaldehyde | HCID 14852334 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3,4,5,6-Tetramethoxy-2-methylphenyl)-1-(3-benzyloxyphenyl)methanol | HCID 22054190 | 95% |
Reaction Steps
An anhydrous tetrahydrofuran (50 ml) solution of 3,4,5,6-tetramethoxy-2-methylbenzaldehyde (14 g, 0.058 mol) was added dropwise under ice cooling to a Grignard reagent (150 ml tetrahydrofuran solution) prepared from 3-(benzyloxy)bromobenzene (18.4 g, 0.070 mol) and magnesium (1.87 g, 0.077 mol), and the resulting solution was stirred for 2 hours. The reaction solution was poured in an aqueous solution of saturated ammonium chloride and extracted with ether. The extract was washed with saturated brine and then dried. The reaction solution was filtered, the filtrate was concentrated and the obtained crude product was purified by silica gel column chromatography (hexand:ethyl acetate=4:1) to obtain the titled compound (23.5 g, 0.055 mol, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07064124B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-90161aa5746a4560a61d570802f2a027 |
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| Source note | uspto-grants-2006_06 |
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