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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Diphenylmethylene-Glycine benzyl ester | HCID 11782449 | — |
| Reactant | cis-2,5-Bis(hydroxymethyl)tetrahydrofuran ditosylate | HCID 86755706 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(Benzhydrylideneamino)-8-oxabicyclo[3.2.1]octane-3-carboxylic acid benzyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06229025B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-f6ea8c87ebb642fea88ba8eea06142be |
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| Source note | uspto-grants-2001_05 |
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