Methanol → HCID 66673635, compound

HRID 1880801Notes

Reaction equation

HRID 1880801 reaction equation
[CH3:1][O:2][C:3](=[O:16])[C@@H:4]([CH2:9][CH:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1)[CH2:5][C:6](O)=[O:7].B.CO>O1CCCC1>[CH3:1][O:2][C:3](=[O:16])[C@@H:4]([CH2:9][CH:10]1[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15]1)[CH2:5][CH2:6][OH:7]

Participants

5

Procedure

A mixture of (S)-2-cyclohexylmethyl-succinic acid 1-methyl ester (60.0 g, 263 mmol) and tetrahydrofuran (600 mL) was stirred at room temperature and then cooled to −5° C. over 30 min. To the reaction mixture was added 1.0 M borane in tetrahydrofuran (520 mL) dropwise over 45 min, keeping the internal temperature below 0° C. To the reaction mixture was added MeOH (100 mL) dropwise to quench the reaction. The reaction mixture was concentrated to about 100 mL by rotary evaporation. (Trifluoromethyl)benzene (200 mL) was added and volume was reduced to 25 mL by rotary evaporation. (Trifluoromethyl)benzene (100 mL) was added to the resulting thick oil and the volume was reduced to ˜25 mL to provide crude title product (56.3 g).

Workup

  1. temperaturecooled to −5° C. over 30 min
  2. customthe internal temperature below 0° C
  3. customto quench
  4. customthe reaction
  5. concentrationThe reaction mixture was concentrated to about 100 mL by rotary evaporation
  6. addition(Trifluoromethyl)benzene (200 mL) was added
  7. customvolume was reduced to 25 mL by rotary evaporation
  8. addition(Trifluoromethyl)benzene (100 mL) was added to the resulting thick oil

Sources & evidence

ORD record
ord-6f2c0a3b38f54b3a9d220658e1c65ae4
Source dataset
uspto-grants-2012_11
Patent number
US08318765B2

Reaction notes

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