HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Pyridine → 3-n-Butyl-5-(4-cyanobenzyl) hydantoin

HRID 1733311
Notes
Print preview

Reaction equation

HRID 1733311 reaction equation
FC(F)(F)C([NH:5]OC(=O)C(F)(F)F)=O.N1C=CC=CC=1.[CH2:21]([N:25]1[C:29](=[O:30])[CH:28]([CH2:31][C:32]2[CH:37]=[CH:36][C:35]([CH:38]=O)=[CH:34][CH:33]=2)[NH:27][C:26]1=[O:40])[CH2:22][CH2:23][CH3:24]>C1C=CC=CC=1>[CH2:21]([N:25]1[C:29](=[O:30])[CH:28]([CH2:31][C:32]2[CH:37]=[CH:36][C:35]([C:38]#[N:5])=[CH:34][CH:33]=2)[NH:27][C:26]1=[O:40])[CH2:22][CH2:23][CH3:24]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 1049PyridineHCID 69634(2,2,2-Trifluoroacetyl)azanyl 2,2,2-trifluoroacetateHCID 127907213-n-Butyl-5-(4-formylbenzyl) hydantoin

Product 1

HCID 127907633-n-Butyl-5-(4-cyanobenzyl) hydantoin

Reagents, catalysts & solvents 1

HCID 241BenzeneSolvent

Procedure

The formyl compound (4.3 g., 0.01 mole), N,O-bis (trifluoroacetyl)hydroxylamine (3.6 g., 0.016 mole) and dry pyridine (2.6 ml. 0.032 mole) were mixed in benzene (75 ml) and heated under reflux for 2 hours. After cooling the benzene solution was washed with water (2×50 ml), dried over magnesium sulphate monohydrate and evaporated in vacuo to give an oil which slowly crystallised. This product was further purified by silica gel chromatography and recrystallisation from a small volume of ethyl acetate to give the title compound, yield 2.5 g., m.p. 136° C.

Workup

  1. temperatureheated
  2. temperatureunder reflux for 2 hours
  3. washwas washed with water (2×50 ml)
  4. dry with materialdried over magnesium sulphate monohydrate
  5. customevaporated in vacuo
  6. customto give an oil which
  7. customslowly crystallised
  8. customThis product was further purified by silica gel chromatography and recrystallisation from a small volume of ethyl acetate

Sources & evidence

ORD record
ord-795fd81335034f58b9bf2e05e5ee13c4
Source dataset
uspto-grants-1980_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04241073

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes