Water → 2-(2-Hydroxyethyl)cyclopent-2-en-1-one

The enol acetate of Example 896 is brominated and dehydrobrominated by the method described in Example 13. The crude product is then dissolved in methylene chloride and is added a7 -78°C. to a methylene chloride solution containing about seven molar equivalents of boron tribromide. After 1 hour a -78°C. the solution is allowed to warm to room temperature and is then kept at ambient temperatures for a total of eighteen hours. The mixture is poured into water and extracted with ether. The organic phase is washed with saturated saline solution, then water and is dried. Evaporation of solvents leaves subject product, which is purified by distillation. The combined organic phases are washed with ice cold 5% sodium hydroxide solution, ice cold 5% hydrochloric acid, and saturaated sodium chloride solution, dried with anhydrous magnesium sulfate and taken to dryness. Distillation gives a pale yellow oil; λ max 5.85 μ (carbonyl group).

1. customis then kept at ambient temperatures for a total of eighteen hours
2. extractionextracted with ether
3. washThe organic phase is washed with saturated saline solution
4. dry with materialwater and is dried
5. customEvaporation of solvents
6. customleaves
7. distillationis purified by distillation
8. washThe combined organic phases are washed with ice cold 5% sodium hydroxide solution, ice cold 5% hydrochloric acid
9. dry with materialdried with anhydrous magnesium sulfate
10. distillationDistillation
11. customgives a pale yellow oil

ORD record

ord-ec4d55a8e9d64162aaacd6da0fb18f9d

Source dataset

uspto-grants-1976_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US03966773