HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819960Generated: November 1, 2026
Phosphorus tribromide → HCID 86605565, compound
https://huagongshe.com/reaction/1819960
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | HCID 57890157 | HCID 57890157 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86605565 | HCID 86605565 | — |
Reaction Steps
To a 0° C. solution of {4-[1-ethyl-1-(4-methyl-thiophen-2-yl)-propyl]-2-methyl-phenyl}-methanol (6 g,) in THF (50 ml) is treated with PBr3 (2.2 ml, 23.3 mmol) and warmed to RT. After stirring for 2 h, the mixture is partitioned between EtOAc and brine. The organic layer is MgSO4 dried, concentrated, and dissolved in anhydrous THF (30 ml) to give a solution of {4-[1-ethyl-1-(4-methyl-thiophen-2-yl)-propyl]-2-methyl-phenyl}-methane bromide. Separately, a solution of 3,3-dimethyl-butan-2-one (5.3 ml, 42.4 mmol) in THF (15 ml) is treated with LiHMDS (42.4 ml, 42.4 mmol, 1M in THF) at −70° C. for 1 h. This solution is transferred (via cannula) into a −70° C. solution of {4-[1-ethyl-1-(4-methyl-thiophen-2-yl)-propyl]-2-methyl-phenyl}-methanebromide/THF. The mixture is warmed to RT and stirred for 1 h. The reaction is diluted with EtOAc and washed with 0.2 N HCl until the aq layer is pH 2. The organic layer is concentrated to give the title compound (6.2 g, 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601850B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-ba647541c1984f15aacd342012d78a66 |
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| Source note | uspto-grants-2009_10 |
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