Sodium borohydride → HCID 57969111, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[O:12][C:13]1[CH:18]=[CH:17][C:16]([B:19]2OC(C)(C)C(C)(C)[O:20]2)=[C:15]([CH:28]=[O:29])[CH:14]=1)[C:5]([O:7][CH3:8])=[O:6].[BH4-].[Na+]>CO>[OH:20][B:19]1[C:16]2[CH:17]=[CH:18][C:13]([O:12][C:11]3[CH:10]=[CH:9][C:4]([C:5]([O:7][CH3:8])=[O:6])=[CH:3][C:2]=3[F:1])=[CH:14][C:15]=2[CH2:28][O:29]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of methyl 3-fluoro-4-(3-formyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)benzoate (5 g, 12.5 mmol) in MeOH (125 mL) was added NaBH4 (709 mg; 18.75 mmol) in portions under N2 at 0° C. in an ice-bath. The reaction was stirred at 0° C. to room temperature. The reaction was monitored with TLC and was completed overnight. The mixture was cooled to rt. Solvent was evaporated to half volume via Rota vapor. The mixture was then cooled to 0° C., and quenched by adding water (12 mL) following by adding 6 N HCl (12 mL). Stirred at rt for 30 min, white Solid precipitated out. Filtered. The solid was gummy. The solid was suspended in water, sonicated for 1 hr. Filtered, washed with more water. Filtered, dried to get white solid. D139 (2.1 g). Yield 55.7%. M.p. 149-152° C. MS (ESI): m/z=303 (M+1, positive) and 301 (M−1, negative). HPLC (220 nm): 97.27% purity. (254 nM): 97.29% purity 1H NMR (DMSO-d6, 300 MHz): δ=9.19 (s, 1H), 7.88 (dd, J=1.8, 11.1 Hz, 1H), 7.80 (d, J=8.4 Hz, 1H), 7.75 (d, J=8.1 Hz, 1H), 7.21 (d, J=8.4 Hz, 1H), 7.07 (d, J=8.4 Hz, 2H), 4.93 (s, 2H), and 3.84 (s, 3H).
Workup
- customSolvent was evaporated to half volume via Rota vapor
- temperatureThe mixture was then cooled to 0° C.
- customquenched
- additionby adding water (12 mL)
- additionby adding 6 N HCl (12 mL)
- stirringStirred at rt for 30 min
- customwhite Solid precipitated out
- filtrationFiltered
- customsonicated for 1 hr
- filtrationFiltered
- washwashed with more water
- filtrationFiltered
- customdried
- customto get white solid
Sources & evidence
- ORD record
- ord-8d996f19492244d49ace04b7956cc4ba
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08039450B2
Reaction notes
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