HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129312Generated: October 27, 2026
Diethyl Ether → 2,2-Di(benzylthiomethyl)pentanal
https://huagongshe.com/reaction/129312
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2,2-Di(benzylthiomethyl)pentan-1-ol | HCID 19373328 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2-Di(benzylthiomethyl)pentanal | HCID 19373415 | — |
Reaction Steps
A solution of 2,2-di-(benzylthiomethyl)pentan-1-ol (1.0 g Example XI) in dry dichloromethane (10 ml) was added to a stirred suspension of pyridinium chlorochromate (1.5 g) and anhydrous sodium acetate (0.11 g) in dry dichloromethane (25 ml) at 0° C., under a current of nitrogen. The reaction mixture was allowed to warm to 20° C. and then stirred for 2 hours. Dry diethyl ether was added and the mixture stirred for 30 minutes. The ethereal extracts were decanted off and the residue was washed with further portions of diethyl ether. The combined ethereal extracts were dried over anhydrous magnesium sulphate and the solvent was removed in vacuo. The residue was purified by chromatography on a mixture of silica and charcoal, eluting with diethyl ether. 2,2-Di(benzylthiomethyl)pentanal was obtained as a pale yellow oil (0.27 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05466710 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-6d1d7433fbd64c8d934a486f6715ca7b |
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| Source note | uspto-grants-1995_11 |
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