تفاعل #81553

ord-47473cc55f5644b6b19ec0dd75be0af0

معادلة التفاعل

[K+].[OH-]
KOH
CN(C)C(=S)Cl
N,N-dimethylthiocarbamoyl chloride
CC1(C)CCC(=O)c2cc(O)ccc21
4,4-dimethyl-7-hydroxy-1-tetralone
CC1(C)CCC(=O)c2cc(O)ccc21
4,4-Dimethyl-7-hydroxy-1-tetralone
[K+].[OH-]
potassium hydroxide
CN(C)C(=S)Oc1ccc2c(c1)C(=O)CCC2(C)C
title product
CN(C)C(=S)Oc1ccc2c(c1)C(=O)CCC2(C)C
4,4-Dimethyl-7-[(dimethylamino)thiocarbonyloxy]-1tetralone

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةcooled below 10° C.
  2. 2
    أخرىkept below 12° C
  3. 3
    أخرىreaction mixture
  4. 4
    استخلاصProduct is extracted with ethyl acetate (2×50 mL), organic phases
  5. 5
    تركيزconcentrated in vacuo
  6. 6
    أخرىthe residue chromatographed on silica gel (eluted with 10% ethyl acetate in hexane)

الإجراء التجريبي

To a solution of 4,4-dimethyl-7-hydroxy-1-tetralone (XIV) (3.07 g, 16.16 mmol) in water (10.77 mL) containing potassium hydroxide (904 mg) cooled below 10° C. was added N,N-dimethylthiocarbamoyl chloride (2.67 g, 21.6 mmol) in tetrahydrofuran (4.30 mL); the reaction temperature kept below 12° C. After 10 minutes, reaction mixture is made basic by the addition of a 10% aqueous KOH solution (5.39 mL). Product is extracted with ethyl acetate (2×50 mL), organic phases concentrated in vacuo and the residue chromatographed on silica gel (eluted with 10% ethyl acetate in hexane) to give 3.74 g (Y: 84%) of title product; 1H-NMR (CDCl3): δ7.68 (d, J=2.6 Hz, 1H), 7.45 (d, J=8.5 Hz, 1H), 7.27 (dd, J=8.5, 2.6 Hz, 1H), 3.46 (s, 3H), 3.34 (s, 3H), 2.73 (t, J=6.8 Hz, 2H), 2.04 (t, J=6.8 Hz, 2H), 1.41 (s, 6H); MS (DCI) m/e: 278 (MH+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05618839uspto-grants-1997_04