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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380640Generated: October 31, 2026

HCID 14302855, compound → HCID 57311524, compound

https://huagongshe.com/reaction/380640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14302855HCID 14302855—
ReactantHCID 54380136HCID 54380136—
SolventPyridineHCID 1049—
ProductHCID 57311524HCID 5731152447.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of (2R)-5-t-butyldiphenylsiloxy-2-hydroxy-2-(hydroxymethyl)-1,2,3,4-tetrahydronaphthalene (0.49 g) and N,N-di(4-fluorophenyl)carbamoyl chloride (1.08 g) in pyridine (2.3 ml) was stirred at 100° C. for 1.5 hours. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with water, 1N-HCl, and evaporated in vacuo. The residue was purified by chromatography on silica gel (50 ml) using a mixture of AcOEt and n-hexane to give (2R)-5-t-butyldiphenylsiloxy-2-{[N,N-di(4-fluorophenyl)-carbamoyloxy]methyl}-2-hydroxy-1,2,3,4-tetrahydronaphthalene (0.356 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06303649B1
Source datasetuspto-grants-2001_10
ORD IDord-f638709005ae4901ab614fb031866db8
Source noteuspto-grants-2001_10