Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List 2,6-DICHLOROPHENYL ISOTHIOCYANATE

2,6-DICHLOROPHENYL ISOTHIOCYANATE synthesis

10synthesis methods
-

Yield: 70%

Reaction Conditions:

with N-ethyl-N,N-diisopropylamine in dichloromethane at 0 - 20;

Steps:

Intermediate of Example-7k: 1, 3-Dichloro-2-isothiocyanatobenzene (15)
N, N-Diisopropylethylamine (1.86 g, 18.41 mmol) was added slowly to a stirred solution of 2, 6-dichloroaniline (2 g, 12.34 mmol) in DCM (25 mL) at room temperature and then cooled to 0 oC. Then, thiophosgene (11.4 g, 13.55 mmol) was added dropwise at that temperature and further stirred at room temperature for 3-4 h. After the reaction completion, the reaction mixture was diluted with water and extracted with DCM. The organic portion was dried over Na2SO4, concentrated and purified by flash column using 5% EtOAc in hexane to afford 1, 3-dichloro-2-isothiocyanatobenzene (1.75 g) in 70% yield. 1H NMR (DMSO-d6): δ 7.39 (t, J = 7.8 Hz, 1H), 7.62 (d, J = 7.8 Hz, 2H).

References:

Muthukaman, Nagarajan;Tambe, Macchindra;Deshmukh, Sanjay;Pisal, Dnyandeo;Tondlekar, Shital;Shaikh, Mahamadhanif;Sarode, Neelam;Kattige, Vidya G.;Pisat, Monali;Sawant, Pooja;Honnegowda, Srinivasa;Karande, Vikas;Kulkarni, Abhay;Behera, Dayanidhi;Jadhav, Satyawan B.;Sangana, Ramchandra R.;Gudi, Girish S.;Khairatkar-Joshi, Neelima;Gharat, Laxmikant A. [Bioorganic and Medicinal Chemistry Letters,2017,vol. 27,# 23,p. 5131 - 5138] Location in patent:supporting information

2,6-DICHLOROPHENYL ISOTHIOCYANATE Related Search: