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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989283Generated: October 29, 2026

Benzyl Bromide → HCID 18005882, compound

https://huagongshe.com/reaction/989283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 18005866HCID 18005866—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18005882HCID 180058826.9%

Reaction Steps

A solution of ethyl 6-chloro-7-hydroxychroman-2-carboxylate (3.0 g, 11.7 mmol) in THF is treated with NaH (3.0 equiv, 35 mmol) at 0° C., stirred for 20 minutes, treated with benzylbromide (3.0 g, 17.5 mmol), stirred for 16 hr, concentrated and diluted with water and EtOAc. The aqueous phase is separated, acidified to pH 1-2 with 2N HCl and extracted with EtOAc. The extracts are combined, dried over MgSO4 and concentrated in vacuo. The resultant residue is dissolved in methanol, treated with a catalytic amount of p-toluenesulfonic acid, heated at reflux temperature for 18 hr, cooled and concentrated in vacuo. This resultant residue is triturated under EtOAc/hexanes and filtered. The filtercake is further purified by short-column chromatography (silica gel, 5:1 hexane:EtOAc as eluent) to afford the title product as a light yellow solid, 2.7 g (6.9% yield), identified by NMR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638972B2
Source datasetuspto-grants-2003_10
ORD IDord-63c147b2fbc4415ead82ff5f7bf0c4af
Source noteuspto-grants-2003_10