Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 57435093 | HCID 57435093 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11845654 | HCID 11845654 | 87.6% |
Reaction Steps
Freshly prepared aq. NaOH (10 M in H2O, 11.85 mmol) was added to a stirring, room temperature solution of 50 (0.0.5269 g, 2.37 mmol) in MeOH (5.9 mL, 0.4 M) under N2. The reaction was then heated to reflux until the reaction was judged complete by HPLC (5 min): The reaction was concentrated, redissolved in H2O, and extracted with EtOAc. 10% aq. HCl was added dropwise to the aqueous layer until the pH=2. The white solid that precipitated from the reaction was filtered off and washed with cold H2O. The solid was dried under vacuum overnight to obtain 0.4034 g (87.6%) of 51. 1H (CD3OD, 400 MHz): δ 6.56 (1H, s), 5.14 (1H, t), 2.68 (2H, t, J=7.3 Hz), 2.33 (2H, q, J=7.3 Hz), 1.67 (3H, s), 1.56 (3H, s) ppm. 13C (CD3OD, 100 MHz): δ 164.94, 148.55, 143.23, 123.94, 107.32, 28.89, 27.04, 25.85, 17.69 ppm. DEPT (CD3OD, 100 MHz): CH3 carbons: 25.85, 17.69; CH2 carbons: 28.89, 27.04; CH carbons: 123.94, 107.32 ppm: HPLC: 8.475 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893098B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-63ec2ea0cc504130ba83a63e7287454a |
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| Source note | uspto-grants-2011_02 |
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