HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994394Generated: November 1, 2026
Sulfuric Acid → 3-(4-(3,3-Dichloro-2-propenyloxy)phenoxy)-1-propyl alcohol
https://huagongshe.com/reaction/1994394
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Bromo-1-propanol | HCID 12308 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(3,3-Dichloro-2-propenyloxy)phenol | HCID 11172014 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(4-(3,3-Dichloro-2-propenyloxy)phenoxy)-1-propyl alcohol | HCID 86633038 | 98.8% |
Reaction Steps
A mixture of 1.40 g of 3-bromopropanol, 10.0 g of toluene and 0.14 g of tetra-n-butylammonium bromide was heated to 60° C. Thereto was added dropwise a mixed solution of 2.0 g of 4-(3,3-dichloro-2-propenyloxy)phenol, 10.0 g of water and 1.49 g of a 27% aqueous sodium hydroxide solution with stirring over 6 hours. After completion of the addition, the mixture was further stirred for 11 hours at 60° C. In this period, 0.20 g of 3-bromopropanol and 0.20 g of a 27% aqueous sodium hydroxide solution were further added at the time point of 7 hours. Then, the reaction mixture was cooled to 20° C. After 4.0 g of a 20% aqueous sulfuric acid solution and 5.0 g of toluene were added thereto, the mixture was stirred and then separated. The obtained organic layer was washed once with 10.0 g of a 1% aqueous sodium hydroxide solution and once with 10.0 g of water, and concentrated under reduced pressure to give 2.5 g of 3-(4-(3,3-dichloro-2-propenyloxy)phenoxy)-1-propyl alcohol (purity: 93%, yield: 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652177B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-38d71269f14b49ab84f60206520d7f8a |
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| Source note | uspto-grants-2010_01 |
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