HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52259Generated: October 28, 2026
Benzyl Bromide → HCID 54247483, compound
https://huagongshe.com/reaction/52259
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3R)-8-bromo-5-methoxychroman-3-amine | HCID 22871216 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54247483 | HCID 54247483 | 155.5% |
Reaction Steps
(R)-3-Amino-8-bromo-5-methoxy-3,4-dihydro-2H-1-benzopyran (11.5 g, 44 mmol) was dissolved in 400 mL anhydrous acetonitrile and to the reaction were benzyl bromide (13 mL, 110 mmol), anhydrous potassium carbonate (grounded) (16 g, 116 mmol), and a catalytic amount of KI added and then heated to 85° C. for 48 h. The solvent was removed in vacuo, the remains were taken into a 2M solution of NH3 and then extracted twice with ether. The combined ether portions were treated with brine, dried (MgSO4), filtered, and the solvent removed in vacuo to give the crude residue. Chromatography on silica (eluent: CH2Cl2) gave 15 g (78% yield) of the title compound as a clear oil. [α]21D =-15.5° (C=0.1 CHCl3) GC-MS (70eV) M=437 (15%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616610 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-e26526080f754ba2a9e1f28760042046 |
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| Source note | uspto-grants-1997_04 |
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