تفاعل #992752

معادلة التفاعل

tert-butyl hypochlorite

phosphate

Sodium hydroxide

4-fluorostyrene

carbamic acid tert-butyl ester

→

title compound

المردود 57.0%

[2-(4-Fluoro-phenyl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester

المردود 57.0%

المذيبات

water

acetonitrile

acetonitrile

water

acetonitrile

ظروف التفاعل

المعالجة

1. 1
   أخرىThe reaction was quenched
2. 2
   أخرىThe phases were separated
3. 3
   استخلاصthe aqueous layer extracted with ethyl acetate (3×20 mL)
4. 4
   غسيلThe combined organic phases were washed with water (1×50 mL)
5. 5
   تجفيفdried over sodium sulfate
6. 6
   تركيزconcentrated in vacuo
7. 7
   أخرىpurified by flash chromatography

الإجراء التجريبي

To a stirred solution of carbamic acid tert-butyl ester (0.22 g) in acetonitrile (6 mL) was added in sequence at 0° C.: Sodium hydroxide (52 mg) in water (5 mL); after 2 minutes tert-butyl hypochlorite (139 μL); after 10 minutes potassium osmate(VI) dihydrate (9 mg) in water (1 mL); after 1 minute hydroquinine (anthraquinone-1,4-diyl)diether (26 mg) in acetonitrile (4 mL); after 3 minutes acetonitrile (6.7 mL) and phosphate buffer (3.3 mL, 0.5 M pH 7.65); after 5 minutes enough sodium biphosphate monohydrate to make pH=7.65; and finally 4-fluorostyrene. The reaction was quenched after stirring 3 hours at 25° C. with sodium sulfite (0.20 g) in water (2 mL) at 0° C. The phases were separated and the aqueous layer extracted with ethyl acetate (3×20 mL). The combined organic phases were washed with water (1×50 mL), dried over sodium sulfate, concentrated in vacuo and purified by flash chromatography to furnish 90 mg (57%) of the title compound as a colorless oil.

المصدر