Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 67430702 | HCID 67430702 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | HCID 11270901 | HCID 11270901 | — |
Reaction Steps
To a solution of 13 (2.2 g, 4.7 mmol) in 50 mL of THF/MeOH (1:1), cooled to 0° C., 1N NaOH solution (55 mL, 32 mmol) was added. The reaction was stirred at 0° C. for 2 h and then overnight at rt. The reaction mixture was concentrated and diluted with H2O (20 mL), cooled to 0° C., acidified to pH 2 with 1N KHSO4 solution and extracted with EtOAc (3×20 mL). The combined organic layers were washed with NaCl (50 mL, sat), dried (Na2SO4), filtered and evaporated. The resulting acid 14 was obtained as a colorless oil (1.76 g, 86%) and used directly in the next step. 1H-NMR (500 MHz, CDCl3): 0.86 (m, 3H), 0.95 (d, J=6.7 Hz, 3H), 1.04-1.14 (m, 21H), 1.90-2.00 (m, 1H), 2.52-2.72 (m, 2H), 3.60-3.62 (m, 1H), 4.28-4.36 (m, 1H), 5.02 (d, J=10.4 Hz, 1H), 5.07-5.13 (m, 3H), 7.25-7.35 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08030279B2 |
|---|
| Source dataset | uspto-grants-2011_10 |
|---|
| ORD ID | ord-61142f32c8f749eaa5d6fef7f426564f |
|---|
| Source note | uspto-grants-2011_10 |
|---|