Hydrochloric Acid → 2-Chloro-5-pyrimidinecarbonitrile

温度

0 °C

(Prepared according to: Organic Synthesis, Vol 4, p. 182.) In a 3-necked, round-bottom flask is placed 5.4 mL of concentrated HCl (65 mmol). The solution is cooled to 0° C. and 2-amino-5-cyanopyrimidine (515 mg, 4.28 mmol) is added portion wise with stirring until a homogeneous solution is obtained. The solution is then cooled to −15° C. A 100 mL addition funnel is fitted to the flask and a cold solution of NaNO2 (592 mg, 8.6 mmol) in 5 ml of water is then added dropwise with stirring over period of 20 min. (The temperature is kept at −15 to −10° C.) The solution is stirred an additional hour and the temperature is allowed to rise to −5. At this point, the mixture is carefully neutralized to about pH 7 with a 30% solution of NaOH, taking care that the temperature does not rise above 0° C. The solution is extracted with EtOAc (3×20 ml), dried over MgSO4, filtered and evaporated to give a yellow solid (159 mg, 21.3% yield).

1. custom(Prepared according to: Organic Synthesis, Vol 4, p. 182.) In a 3-necked, round-bottom flask
2. customis obtained
3. temperatureThe solution is then cooled to −15° C
4. additionA 100 mL addition funnel
5. customis fitted to the flask
6. stirringwith stirring over period of 20 min. (The temperature
7. customis kept at −15 to −10° C.
8. stirringis stirred an additional hour
9. customdoes not rise above 0° C
10. extractionThe solution is extracted with EtOAc (3×20 ml)
11. dry with materialdried over MgSO4
12. filtrationfiltered
13. customevaporated

ORDレコード

ord-444a33122d1646e8b7c0df71ec2b5fbe

出典データセット

uspto-grants-2013_09

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08536168B2