HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035397Generated: October 30, 2026
Carbon tetrabromide → HCID 67416796, compound
https://huagongshe.com/reaction/2035397
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 67418345 | HCID 67418345 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67416796 | HCID 67416796 | 79.5% |
Reaction Steps
To a solution of the product from step D (0.36 g, 0.46 mmol) in tetrahydrofuran (5.0 mL) at 0° C. was added triphenylphosphine (0.36 g, 1.38 mmol), followed by dropwise addition of a solution of carbon tetrabromide (0.46 g, 1.38 mmol) in tetrahydrofuran (5.0 mL). The reaction mixture was allowed to warm to room temperature and stirred for 8 hours. The reaction solution was then quenched by addition of methanol and stirred for 15 minutes at room temperature. The resultant mixture was concentrated to dryness and the residue obtained was purified by flash column chromatography (eluent: hexanes/ethyl acetate 95:5 to 60:40) to give (2S,3R,4R,5R)-2-(3-(bromomethyl)-4-chlorophenyl)-3,4,5-tris(4-methoxybenzyloxy)-6-((4-methoxybenzyloxy)methyl)tetrahydro-2H-pyran (0.31 g, partial pure) as a light yellow oil, which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08575114B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-4e68f4d9444f4bd6ad2fa690d467aa76 |
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| Source note | uspto-grants-2013_11 |
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