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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035397Generated: October 30, 2026

Carbon tetrabromide → HCID 67416796, compound

https://huagongshe.com/reaction/2035397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 67418345HCID 67418345—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67416796HCID 6741679679.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575114B2
Source datasetuspto-grants-2013_11
ORD IDord-4e68f4d9444f4bd6ad2fa690d467aa76
Source noteuspto-grants-2013_11