HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54763Generated: October 29, 2026
Ammonium Chloride → 1-(Benzyloxy)pent-4-en-2-ol
https://huagongshe.com/reaction/54763
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (Phenylmethoxy)acetaldehyde | HCID 108989 | — |
| Reactant | HCID 178455850 | HCID 178455850 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(Benzyloxy)pent-4-en-2-ol | HCID 10035478 | — |
Reaction Steps
To a stirring 0° C. solution of 59.0 g of product from Example 1 in 375 ml of diethyl ether is added, dropwise, 432.24 ml of 1M allylmagnesium bromide in ether. The reaction is stirred at 0° C. for 1 hour, followed by overnight stirring at room temperature. The reaction is cooled to 0° C., hydrolyzed with saturated ammonium chloride, and the layers are separated. The organic layer is washed with saturated sodium chloride, dried and concentrated in vacuo to give the product as an oil. The crude oil is purified by Kugelrohr distillation (bath temperature 100° C.) to give 61.5 g of the desired product as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05623081 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-8d08157a102b4f9c89a6a53c15e800da |
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| Source note | uspto-grants-1997_04 |
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