Methanol → HCID 57508887, compound

HRID 2240795Notes

Reaction equation

HRID 2240795 reaction equation
[CH:1]([C:3]1[S:7][C:6]([C:8]([OH:10])=[O:9])=[C:5]2[CH2:11][CH2:12][C:13]([CH3:16])([CH3:15])[CH2:14][C:4]=12)=[O:2].CO>C(O)(=O)CC(CC(O)=O)(C(O)=O)O.[Cl-].[Na+].O>[OH:2][CH2:1][C:3]1[S:7][C:6]([C:8]([OH:10])=[O:9])=[C:5]2[CH2:11][CH2:12][C:13]([CH3:16])([CH3:15])[CH2:14][C:4]=12

Participants

5

Procedure

To a solution of crude 3-formyl-5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid (2.38 g, 10 mmol) in methanol (20 mL) NaBH4 (756 mg, 20 mmol) is added in portions. The mixture is stirred at rt for 15 min, diluted with 10% aq. citric acid and brine and extracted with TBME. The organic extract is dried over Na2SO4 and the solvent is removed under reduced pressure to give 3-hydroxymethyl-5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid (2.30 g) as a beige foam; LC-MS: tR=0.83 min, [M+1]=241.22; 1H NMR (CDCl3): δ 4.69 (s, 2H), 3.00 (t, J=7.0 Hz, 2H), 2.32 (s, 2H), 1.50 8 t, J=7.0 Hz, 2H), 0.94 (s, 6H).

Workup

  1. extractionextracted with TBME
  2. extractionThe organic extract
  3. dry with materialis dried over Na2SO4
  4. customthe solvent is removed under reduced pressure

Sources & evidence

ORD record
ord-d0eefe9ac3024376875598f64f4826bc
Source dataset
uspto-grants-2010_05
Patent number
US07723378B2

Reaction notes

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