HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564444Generated: October 31, 2026
Dimethyl Sulfide → (3-Bromo-2-fluorophenyl)methanamine
https://huagongshe.com/reaction/564444
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | 3-Bromo-2-fluorobenzamide | HCID 44203102 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Bromo-2-fluorophenyl)methanamine | HCID 12084140 | 46.3% |
Reaction Steps
To a solution of 3-bromo-2-fluorobenzamide (3.0 g, 13.76 mmol) in THF (50 mL) was added BH3.Me2S (1.57 mL, 20.6 mmol) and stirred at 50° C. for 2 h (monitored by TLC). The reaction was quenched by adding HCl (20 mL, 3 N) and the result mixture was stirred for 2 h before THF was removed under vacuum. The aqueous layer was extracted with AcOEt (30 mL), and then was adjusted to pH=9.0 with NaOH (1 N). The aqueous layer was extracted with AcOEt (50 mL×2). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated to give 1.30 g of the title compound, as a colorless oil (yield: 46%). 1H NMR (400 MHz, D2O): δ 4.30 (S, 2 H), 7.19-7.22 (m, 1 H), 7.47 (t, J=8.8 Hz, 1 H), 7.73-7.77 (m, 1 H); 13C NMR (100 MHz, D2O): δ 37.4, 108.9, 121.2, 126.2, 130.7, 135.1, 156.2, 158.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067408B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-8a420ac046aa49be843f7bcb0af779ba |
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| Source note | uspto-grants-2011_11 |
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