Dichloromethane → HCID 21450746, compound

HRID 372791Notes

Reaction equation

HRID 372791 reaction equation
[C:1]1([C:7]2([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[O:13][CH2:12][CH2:11][NH:10][CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:20](Br)[CH:21]=[CH2:22].C(=O)(O)[O-].[Na+].C(Cl)[Cl:30]>>[ClH:30].[CH2:22]([N:10]1[CH2:9][CH2:8][C:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)([C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[O:13][CH2:12][CH2:11]1)[CH:21]=[CH2:20]

Participants

5

Reactant 4

HCID 6344DichloromethaneHCID 7841Allyl bromideHCID 516892Sodium BicarbonateHCID 203266297,7-Diphenyl-1,4-oxazepane

Product 1

HCID 21450746HCID 21450746, compound

Procedure

To the stirred solution of 5.06 g of 7,7-diphenyl-hexahydro-1,4-oxazepine in 50 ml of methylene chloride, 2.6 g of allyl bromide are added, followed by 40 ml of 10% aqueous sodium bicarbonate and the mixture is stirred for 24 hours at room temperature. The organic layer is separated, washed with water, dried, filtered and evaporated. The residue is taken up in acetone, the solution acidified with hydrogen chloride in acetone and diluted with diethyl ether, to yield the 4-allyl-7,7-diphenyl-hexahydro-1, 4-oxazepine hydrochloride melting at 246° to 247°.

Workup

  1. customThe organic layer is separated
  2. washwashed with water
  3. customdried
  4. filtrationfiltered
  5. customevaporated
  6. additiondiluted with diethyl ether

Sources & evidence

ORD record
ord-86751c8819de4090bee95acde0394f6e
Source dataset
uspto-grants-1978_05
Patent number
US04092330

Reaction notes

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