Sodium Dithionite → HCID 21946139, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]2[C:13](=[CH:14][C:15]=1[CH2:16][CH2:17][C:18]([O:20]C)=[O:19])[N+:12]([O-])=[C:11]1[C:6](=[CH:7][C:8](=[O:23])[CH:9]=[CH:10]1)[O:5]2.S(S([O-])=O)([O-])=O.[Na+].[Na+]>[OH-].[Na+]>[OH:1][C:2]1[CH:3]=[C:4]2[C:13](=[CH:14][C:15]=1[CH2:16][CH2:17][C:18]([OH:20])=[O:19])[N:12]=[C:11]1[C:6](=[CH:7][C:8](=[O:23])[CH:9]=[CH:10]1)[O:5]2Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Methyl ester (10a) (22.83 g, 72.4 mmol) was dissolved in 400 ml of 0.5 M aqueous sodium hydroxide and the solution was stirred for 1 h. A solution of sodium dithionite solution (200 ml, 100 mmol) was added and reaction mixture was stirred for additional 15 minutes. To precipitate the product 3 M hydrochloric acid (80 ml) was carefully added and resultant suspension was stirred for 10 min and centrifuged. The supernatant was decanted and the residue was re-suspended in 800 ml of water and centrifuged again. This operation was repeated one more time. Final supernatant had pH of 3-4. The centrifuged material was dried under vacuum overnight at 40° C. to afford 14.12 g (68%) of desired product (hla) as a brown solid. 1H NMR (CD3OD, +40° C.): δ 7.64 (d, J=9.0 Hz, 1H), 7.39 (s, 1H), 6.89 (d, J=9.0 Hz, 1H), 6.74 (s, 1H), 6.34 (s, 1H), 2H), 2.51 (m, 2H).
Workup
- customreaction mixture
- stirringwas stirred for additional 15 minutes
- customTo precipitate the product 3 M hydrochloric acid (80 ml)
- additionwas carefully added
- stirringresultant suspension was stirred for 10 min
- customThe supernatant was decanted
- customThe centrifuged material was dried under vacuum overnight at 40° C.
Sources & evidence
- ORD record
- ord-1746da25a0b64dd793dc6ef4f4989ea6
- Source dataset
- uspto-grants-2009_10
- Patent number
- US07601851B2
Reaction notes
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