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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976914Generated: November 1, 2026

Sodium hydride → 3-(Benzhydrylideneamino)-8-oxabicyclo[3.2.1]octane-3-carboxylic acid benzyl ester

https://huagongshe.com/reaction/1976914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantDiphenylmethylene-Glycine benzyl esterHCID 11782449—
Reactantcis-2,5-Bis(hydroxymethyl)tetrahydrofuran ditosylateHCID 86755706—
SolventDimethylformamideHCID 6228—
Product3-(Benzhydrylideneamino)-8-oxabicyclo[3.2.1]octane-3-carboxylic acid benzyl esterHCID 54051614—

Reaction Steps

To a suspension of sodium hydride (0.41 grams, 17.1 mmole) in N,N-dimethylformamide (50 mL) at 0° C. is added dropwise a solution of N-diphenylmethylene glycine benzyl ester (7.8 mmole) in N,N-dimethylformamide (50 mL). After stirring for 30 minutes at room temperature, a solution of cis-2,5-bis(hydroxymethyl)-tetrahydrofuran ditosylate (4.1 grams, 9.3 mmole)(prepared by literature methods such as those described in JOC, 47, 2429-2435 (1982)) in N,N-dimethylformamide (50 mL) is added dropwise. The reaction mixture is gradually heated to 100° C. in an oil bath and stirred at this temperature overnight. The solvent is evaporated under vacuum and the residue is taken up in water and extracted twice with diethyl ether. The combined organic extracts are washed with brine, dried over magnesium sulfate and concentrated to a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06229025B1
Source datasetuspto-grants-2001_05
ORD IDord-f6ea8c87ebb642fea88ba8eea06142be
Source noteuspto-grants-2001_05