2-Bromoethanol → HCID 22342574, compound

HRID 584236Notes

Reaction equation

HRID 584236 reaction equation
Cl.[CH2:2]1[C:4]2([CH2:9][O:8][CH2:7][CH2:6][NH:5]2)[CH2:3]1.Br[CH2:11][CH2:12][OH:13].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O.[Cl-].[Na+].O>[OH:13][CH2:12][CH2:11][N:5]1[CH2:6][CH2:7][O:8][CH2:9][C:4]21[CH2:3][CH2:2]2

Participants

6

Conditions

Temperature
90 °C

Procedure

A mixture of 7-oxa-4-azaspiro[2.5]octane hydrochloride (200 mg), 2-bromoethanol (0.28 ml) and potassium carbonate (550 mg) in N,N-dimethylformamide (2 ml) was stirred at 90° C. for 48 hours and cooled. The mixture was poured into brine and extracted with dichloromethane. The extract was dried over magnesium sulfate and evaporated under reduced pressure, and purified by column chromatography on silica gel using a mixture of methanol and chloroform (2:98) to give 4-(2-hydroxyethyl)-7-oxa-4-azaspiro[2.5]octane as an oil. This oil was dissolved in ethyl acetate (5 ml) and the solution was added methanesulfonyl chloride (0.16 ml) and triethylamine (0.3 ml). After 30 minutes of stirring at room temperature, the mixture was filtered, evaporated, and purified by column chromatography on silica gel using a mixture of ethyl acetate and n-hexane (20:80˜30:70) to give 4-(2-chloroethyl)-7-oxa-4-azaspiro[2.5]octane (140 mg) as an oil.

Workup

  1. temperaturecooled
  2. extractionextracted with dichloromethane
  3. dry with materialThe extract was dried over magnesium sulfate
  4. customevaporated under reduced pressure
  5. custompurified by column chromatography on silica gel using
  6. additiona mixture of methanol and chloroform (2:98)

Sources & evidence

ORD record
ord-ccdfaf1d84b4455c9ca95872628ec6fb
Source dataset
uspto-grants-2005_08
Patent number
US06924278B2

Reaction notes

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