1-Methylcyclopentene → HCID 10772975, compound

HRID 1750512

Reaction equation

HRID 1750512 reaction equation
[CH3:1][C:2]1[CH2:6][CH2:5][CH2:4][CH:3]=1.ClS([N:11]=[C:12]=[O:13])(=O)=O.S([O-])([O-])=O.[Na+].[Na+].[OH-].[K+]>C(OCC)C.O>[CH3:1][C:2]12[NH:11][C:12](=[O:13])[CH:6]1[CH2:5][CH2:4][CH2:3]2

Participants

7

Procedure

To a solution of 1-methylcyclopent-1-ene (CAS number 693-89-0; 38.5 mL, 365 mmol) in diethyl ether (220 ml) at 0° C. was added drop wise [(chlorosulfonyl)imino]methanone (CAS number 1189-71-5; 33.3 ml, 383 mmol). The reaction was then allowed to warm to room temperature and then heated to 36° C. for 72 hours. The reaction was then cooled to room temperature and a solution of sodium sulfite (73.5 g) in water (400 ml) was added drop wise, followed by the addition of 15% w/v potassium hydroxide (500 ml) to obtain pH 7-8. The phases were separated and aqueous phase was extracted with diethyl ether (2×200 ml). The combined organics were dried over magnesium sulfate and concentrated in vacuo to afford the title compound.

Workup

  1. temperatureheated to 36° C. for 72 hours
  2. temperatureThe reaction was then cooled to room temperature
  3. additionfollowed by the addition of 15%
  4. customto obtain pH 7-8
  5. customThe phases were separated
  6. extractionaqueous phase was extracted with diethyl ether (2×200 ml)
  7. dry with materialThe combined organics were dried over magnesium sulfate
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-5e70b3aa1f97443bbde24760afcb2e01
Source dataset
uspto-grants-2015_10
Patent number
US09156829B2

Linked notes

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