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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234740Generated: October 25, 2026

Methanol → HCID 15198019, compound

https://huagongshe.com/reaction/234740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant4-(Benzoxazol-2-yl)benzyl bromideHCID 11033515—
ReactantHCID 54395449HCID 54395449—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15198019HCID 15198019—

Reaction Steps

To KH (35%; (0.34 g; 0.0029 mole) in THF (8 ml) under N2 and cooled in an ice bath is added N-trityl-5-hydroxytricyclo-[3.3.1.13,7 ]decan-2-amine (1.0 g; 0.0025 mole) This forms a pale yellow solution and is stirred at room temperature for 1 hour. The reaction mixture is then cooled in ice and 4-(benzoxazol-2-yl)benzyl bromide (0.7 g; 0.0025 mole) is added all at once. The mixture is stirred for 1/2 hour with ice cooling and then 31/2 hours at room temperature then cooled in ice and MeOH is added to quench the KH. The mixture is evaporated to dryness. Purification is accomplished on HPLC eluting with a gradient system staring with 10% and ending with 20% ethyl acetate/hexane to obtain N-trityl-5-[4-(benzoxazol-2-yl)benzyloxy]tricyclo[3.3.1.13,7 ]decan-2-amine which is used directly in step F.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05596020
Source datasetuspto-grants-1997_01
ORD IDord-5fa2dd0866c642e48a6ba1f0bb23fe99
Source noteuspto-grants-1997_01