HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420286Generated: October 31, 2026
Phosphorus tribromide → HCID 57429690, compound
https://huagongshe.com/reaction/420286
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | HCID 66649617 | HCID 66649617 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 57429690 | HCID 57429690 | — |
Reaction Steps
Phosphorous tribromide (20.9 mL, 218 mmol) was added to diethylether (700 mL) at 0° C. To the PBr3 solution was added dropwise (2-fluoro-4-hydroxymethyl-phenyl)-carbamic acid benzyl ester (36.5 g, 133 mmol) in Et2O (400 mL) at 0° C. over 1 h. The reaction mixture was stirred at room temperature for 45 min and was carefully quenched at 0° C. with MeOH (100 mL). The reaction mixture was diluted with aq. NaHCO3 solution and extracted with EtOAc. The combined organic phases were washed with brine, dried over Na2SO4, filtered and evaporated to provide the title compound as a yellow foam: TLC (cyclohexane-EtOAc 1:1) Rf=0.88; HPLC RtI=1.16 min; 1H NMR (360 MHz, CDCl3): δ 8.13 (t, 1H), 7.48-0.37 (m, 5H), 7.21-7.14 (m, 2H), 6.78 (s broad, 1H), 5.25 (s, 2H), 4.47 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093406B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-365bb718099842198e589241dbab5d9c |
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| Source note | uspto-grants-2012_01 |
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