HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362947Generated: October 27, 2026
2-(Tert-butoxy)ethan-1-ol → 1-(3-Chlorophenyl)-2-(2-tertbutoxyethoxy)ethanol
https://huagongshe.com/reaction/362947
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Tert-butoxy)ethan-1-ol | HCID 24232 | — |
| Reactant | 2-(3-Chlorophenyl)oxirane | HCID 155613 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(3-Chlorophenyl)-2-(2-tertbutoxyethoxy)ethanol | HCID 53835502 | — |
Reaction Steps
5.1 g of potassium tert-butoxide was added to 105 ml of ethylene glycol mono-tert-butyl ether. The mixture was heated to 80° C. Thereto was dropwise added 35.0 g of 2-(3-chlorophenyl)oxirane over 1 hour. The mixture was stirred for 2 hours at the same temperature. The reaction mixture was added to a mixture of 100 ml of ice water and 100 ml of ethyl acetate. The organic layer was separated, washed with a saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue thus obtained was subjected to further distillation under reduced pressure to obtain 37.7 g of colorless oily 1-(3-chlorophenyl)-2-(2-tert-butoxyethoxy)ethanol having a boiling point of 140°-146° C./0.9 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05872117 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-5f4717452211468eb27f84faaf6c163f |
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| Source note | uspto-grants-1999_02 |
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