Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | But-3-enyl 4-methylbenzenesulfonate | HCID 11299102 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54338129 | HCID 54338129 | 13.8% |
Reaction Steps
Into a reactor, 1,3-propanediol (46.7 g) and potassium hydroxide (34.5 g) were charged and stirred, and heated at the internal temperature of 75° C. for 30 minutes. At the internal temperature of 80° C., CH2═CH(CH2)2OTs (69.5 g) obtained in EXAMPLE 3-1 was added thereto over 3 hours and standed as it is after stirring for 1 hour. The reaction mixture was poured into water (250 ml) and neutralized by adding hydrochloric acid. After filtration, the filtrate was extracted with t-butyl methyl ether (300 ml) four times. The organic layer put together was dried over magnesium sulfate and subjected to filtration, and the solvent was distilled off to obtain 5.5 g of CH2═CH(CH2)2O(CH2)3OH.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06833477B2 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-fb42bb7a19e440a895f9ce8b91c1f2c8 |
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| Source note | uspto-grants-2004_12 |
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