Formic Acid → HCID 20316648, compound

HRID 2419021Notes

Reaction equation

HRID 2419021 reaction equation
[Cl:1][C:2]1[C:12]2[CH2:11][CH2:10][NH:9][CH2:8][CH:7]([C:13]3[CH:18]=[CH:17][C:16]([S:19][CH3:20])=[CH:15][CH:14]=3)[C:6]=2[CH:5]=[C:4]([O:21][CH3:22])[C:3]=1[O:23][CH3:24].[OH-].[Na+].[CH:27](O)=O>C=O>[Cl:1][C:2]1[C:12]2[CH2:11][CH2:10][N:9]([CH3:27])[CH2:8][CH:7]([C:13]3[CH:14]=[CH:15][C:16]([S:19][CH3:20])=[CH:17][CH:18]=3)[C:6]=2[CH:5]=[C:4]([O:21][CH3:22])[C:3]=1[O:23][CH3:24]

Participants

5

Procedure

A solution of 4 g of 6-chloro-7,8-dimethoxy-1-(p-methylthiophenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine in 15 ml of formic acid and 10 ml of formaldehyde is refluxed for 18 hours. The reaction mixture is evaporated to dryness, 20 ml of 6N hydrochloric acid is added and the solution is again evaporated to dryness to give a liquid. The latter is treated with 20 ml of 10% sodium hydroxide solution and the mixture is extracted with ether. The dried extract is evaporated to give 6-chloro-7,8-dimethoxy-3-methyl-1-(p-methylthiophenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine.

Workup

  1. customThe reaction mixture is evaporated to dryness, 20 ml of 6N hydrochloric acid
  2. additionis added
  3. customthe solution is again evaporated to dryness
  4. customto give a liquid
  5. extractionthe mixture is extracted with ether
  6. extractionThe dried extract
  7. customis evaporated

Sources & evidence

ORD record
ord-93f08d9875fa4fada696d0633ab8518c
Source dataset
uspto-grants-1978_08
Patent number
US04104379

Reaction notes

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