Methanethiol → Ethyl nitro(1,3-thiazinan-2-ylidene)acetate

HRID 462168Notes

Reaction equation

HRID 462168 reaction equation
CS[C:3]1[S:4][CH2:5][CH2:6][CH2:7][N:8]=1.[N+:9]([CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14])([O-:11])=[O:10].CS>[Cl-].[Zn+2].[Cl-].CCOCC.C(O)(C)C>[N+:9]([C:12](=[C:3]1[NH:8][CH2:7][CH2:6][CH2:5][S:4]1)[C:13]([O:15][CH2:16][CH3:17])=[O:14])([O-:11])=[O:10]

Participants

6

Reactant 3

HCID 878MethanethiolHCID 69379Ethyl nitroacetateHCID 27820812-(methylsulfanyl)-5,6-dihydro-4H-1,3-thiazine

Product 1

HCID 71443329Ethyl nitro(1,3-thiazinan-2-ylidene)acetate

Reagents, catalysts & solvents 2

HCID 3007855ZincchlorideCatalyst3×HCID 22147583Diethyl ether 2-propanolSolvent

Procedure

To a mixture of 235 g of 5,6-dihydro-2-(methylthio)-4H-1,3-thiazine and 2 g of zinc chloride at approximately 115° in a nitrogen atmosphere, 263 g of ethyl nitroacetate was added dropwise over a 1.5 hour period. The mixture was held at 110°-120°. When evolution of methyl mercaptan ceased after 45 minutes further stirring of the heated mixture, 1 g of zinc chloride was added and the mixture was stirred at about 115° for 1.25 hours. An additional 1 g of zinc chloride then was added and stirring of the mixture at about 115° was continued for 1.5 hours. The mixture then was poured into a cooled solution of 2/1 ether/isopropyl alcohol mixture. The crystallized product was collected, washed with ether and dried under reduced pressure to leave a tan solid, m.p. 100°-102°, which on recrystallization from methanol gave 2A as a pale yellow solid, m.p. 105°-106°.

Workup

  1. additionwas added dropwise over a 1.5 hour period
  2. customwas held at 110°-120°
  3. additionwas added
  4. stirringstirring of the mixture at about 115°
  5. waitwas continued for 1.5 hours
  6. customThe crystallized product was collected
  7. washwashed with ether
  8. customdried under reduced pressure
  9. customto leave a tan solid, m.p. 100°-102°, which
  10. customon recrystallization from methanol

Sources & evidence

ORD record
ord-492b556cf2aa44529d1cdf87c4df2d91
Source dataset
uspto-grants-1977_12
Patent number
US04065560

Reaction notes

Loading…