HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607754Generated: October 30, 2026
Benzyl Bromide → ((3-Chloropropoxy)methyl)benzene
https://huagongshe.com/reaction/1607754
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 3-Chloro-1-propanol | HCID 12313 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ((3-Chloropropoxy)methyl)benzene | HCID 221505 | 97.9% |
Reaction Steps
In a 2 l flask, a mixture of 3-chloropropanol (56.7 g), benzyl bromide (102.6 g) and dry THF (600 ml) is stirred and cooled with ice/salt mixture. Potassium tert-butoxide (70 g) is added in portions (5-10 g), maintaining the internal temperature at about 0° C. After the mixture is stirred for 3 more hours at room temperature, the solvent is evaporated. Addition of 1N HCl (1 l), extraction with ether (1 l), and evaporation of solvent gives crude material (113.6 g), which is distilled under vacuum to give 1-chloro-3- benzyloxypropane (108.4 g) b.p.0.01 60°-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04866206 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-10b47b92bf4148578689f32ad145f79c |
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| Source note | uspto-grants-1989_09 |
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