M-Cresol → 2-Hydroxy-4-methylbenzonitrile

Temperature

80 °C

2-Hydroxy-4-methylbenzonitrile was prepared following a modification of the procedure reported by Makoto Adachi and Tsutomu Sugasawa (Synthetic Communications 1990, 20, 71–84.). To a cold (0° C.) solution of BCl3 (1.0 M in heptane, 12.0 mL, 12.0 mmol) in 1,2-dichloroethane was added neat m-cresol (1.00 mL, 9.56 mmol) followed by CH3SCN (0.83 mL, 12.1 mmol) and AlCl3 (1.38 g, 10.4 mmol). The cooling bath was removed and the resultant mixture was heated to 80° C. for 3 hours then cooled to room temperature. The mixture was poured into 4 N NaOH (35 mL) and the mixture was heated at 80° C. for 45 minutes then cooled to room temperature. The phases were separated and the aqueous phase was extracted with CH2Cl2 (3×50 mL). The aqueous phase was acidified with 6 N HCl (30 mL) and extracted with diethyl ether (3×50 mL). The combined ether extracts were dried (MgSO4) and concentrated. Purification of the crude material by column chromatography on silica gel (20:1 CH2Cl2—EtOAc) provided 1.16 g (91%) of 2-Hydroxy-4-methylbenzonitrile as a white solid. 1H NMR (CDCl3) δ 2.36 (s, 3H), 6.20 (br s, 1H), 6.79–6.81 (m, 2H), 7.38 (d, 1H, J=9 Hz).

1. custom2-Hydroxy-4-methylbenzonitrile was prepared
2. customThe cooling bath was removed
3. temperaturethen cooled to room temperature
4. additionThe mixture was poured into 4 N NaOH (35 mL)
5. temperaturethe mixture was heated at 80° C. for 45 minutes
6. temperaturethen cooled to room temperature
7. customThe phases were separated
8. extractionthe aqueous phase was extracted with CH2Cl2 (3×50 mL)
9. extractionextracted with diethyl ether (3×50 mL)
10. dry with materialThe combined ether extracts were dried (MgSO4)
11. concentrationconcentrated
12. customPurification of the crude material by column chromatography on silica gel (20:1 CH2Cl2—EtOAc)

ORD record

ord-1460cafe3e734ae289235f35d72669f6

Source dataset

uspto-grants-2006_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07091217B2