HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10076Generated: October 26, 2026
Dimethylamine → 9,10-Dihydroanthracene
https://huagongshe.com/reaction/10076
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | Sodium chloride; water | HCID 57417360 | — |
| Reactant | 4-{[(4-Hydroxymethyl-phenyl)-methyl-amino]-methyl}-benzoic acid methyl ester | HCID 69520628 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 9,10-Dihydroanthracene | HCID 11940 | — |
Reaction Steps
To an ice cold solution of 4-{[(4-hydroxymethyl-phenyl)-methyl-amino]-methyl}-benzoic acid methyl ester (0.5 g, 1.8 mmol) and 3-isopropenyl-phenyl)-dimethyl-amine (0.31 g, 1.9 mmol) in methylene chloride (CH2Cl2, 25 mL)) is added dropwise a solution of boron trichloride (1 M BCl3 in CH2Cl2, 2 mL). The reaction mixture is allowed to stir overnight at room temperature cooled to −15° C. (NaCl/water) followed by dropwise addition of concentrated sulfuric acid (12 mL). Methylene chloride is removed and the mixture is allowed to stand at 40° C. over a period of 16 h. The resulting solution is poured into crushed ice and neutralized with 2 N sodium hydroxide. The aqueous solution is extracted with methylene chloride (2×75 ml), dried (Na2SO4) and concentrated giving the 9,10-dihydro-anthracene as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091348B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-ca7acc999d4a4b90bdd5cd77f7621709 |
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| Source note | uspto-grants-2006_08 |
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