HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1617398Generated: November 2, 2026
Dimethylamine → Methyl 3-bromo-5-((dimethylamino)methyl)benzoate
https://huagongshe.com/reaction/1617398
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Methyl 3-bromo-5-formylbenzoate | HCID 11436457 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-bromo-5-((dimethylamino)methyl)benzoate | HCID 58187962 | — |
Reaction Steps
To a solution of methyl 3-bromo-5-formylbenzoate (1.8 g, 7.4 mmol, prepared as described in WO 2003048111 from dimethyl 5-bromoisophthalate, Alfa Aesar) in methylene chloride (20 mL) was added a solution of 2.0 M dimethylamine in tetrahydrofuran (7.4 mL, 15 mmol). This mixture was stirred for 15 minutes, followed by the addition of sodium triacetoxyborohydride (4.7 g, 22 mmol). The resulting mixture was stirred overnight. Saturated sodium bicarbonate solution was added and the product was extracted with ethyl acetate. The combined organic extracts were washed twice with water, once with brine, dried over sodium sulfate, filtered and concentrated to afford a light yellow oil. Yield: 1.87 g (93%); LC-MS: 272.0, 274.0 (M+H)+. 1H NMR (400 MHz, CDCl3): δ 8.06 (dd, 1H), 7.89 (dd, 1H), 7.69 (dd, 1H), 3.91 (s, 3H), 3.42 (s, 2H), 2.24 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765734B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-88b9442b4ca740a882603af2b2a1384b |
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| Source note | uspto-grants-2014_07 |
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