Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 1,4-Butanediol | HCID 8064 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Benzyloxy-1-butanol | HCID 562212 | — |
Reaction Steps
42 a of sodium hydride (60% strength) are introduced in portions into 900 ml of abs. DMF at room temperature. 88.6 ml of 1,4-butanediol in 450 ml of abs. DMF are added dropwise to the suspension cooled to −20° C. such that the internal temperature does not exceed −15° C. After addition is complete, a solution of 121 ml of benzyl bromide in 870 ml of abs. DMF is rapidly added dropwise and the reaction mixture is then stirred at room temperature for 30 minutes. The reaction is ended by careful addition of 315 ml of water. For work-up, the reaction mixture is stirred into 1.5 l of water and extracted 3 times with 1 l of ether in each case. The ethereal phases are combined, washed with water, dried over magnesium sulphate and concentrated in vacuo. Chromatography on silica gel using a hexane-ethyl acetate gradient yields 105 g of 4-benzyloxybutan-1-ol as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06677324B1 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-ad94809c2f49424787a0407ff105a930 |
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| Source note | uspto-grants-2004_01 |
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