Sodium Hydroxide → 2-nitromethylenetetrahydro-2H-1,3-thiazine

HRID 461001Notes

Reaction equation

HRID 461001 reaction equation
[N+:1]([C:4](=[C:10]1[NH:15][CH2:14][CH2:13][CH2:12][S:11]1)C(OCC)=O)([O-:3])=[O:2].[OH-].[Na+]>C(O)(=O)C>[N+:1]([CH:4]=[C:10]1[NH:15][CH2:14][CH2:13][CH2:12][S:11]1)([O-:3])=[O:2]

Participants

4

Procedure

2.3 G OF 1A was added to 10 ml of 20% aqueous sodium hydroxide and the mixture was stirred at room temperature for 12 hours. The resulting solution was treated dropwise with 3.5 g of acetic acid. The addition was accompanied by vigorous gas evolution. The resulting mixture was extracted with methylene chloride and the extract was dried (magnesium sulfate) and concentrated under reduced pressure to give tetrahydro-2--(nitromethylene)-2H-1,3-thiazine (1B) as a pale yellow solid, m.p. 76°-78°.

Workup

  1. additionThe addition
  2. extractionThe resulting mixture was extracted with methylene chloride
  3. dry with materialthe extract was dried (magnesium sulfate)
  4. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-97666166536f44f2b90750109a5f3719
Source dataset
uspto-grants-1977_12
Patent number
US04061749

Reaction notes

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