Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 88182850 | HCID 88182850 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131723723 | HCID 131723723 | — |
Reaction Steps
Thioacetic acid S-(trans-3-tert-butoxycarbonylamino-6-tert-butoxycarbonyloxy-4,4-diethyl-1,2,3,4-tetrahydro-naphthalen-2-yl) ester (234 mg, 0.47 mmol) in MeOH (5 mL) was added the sodium methoxide (54 μL, 0.95 mmol) and stirred at 0° C. for 30 min. The mixture was quenched with H2O, diluted with Et2O (50 mL), washed with H2O, HCl (10%), H2O, brine, dried over MgSO4. The residu was used without any other purification (151 mg, 71%). 1H NMR (CDCl3): 7.10-6.95 (3H, m, Har), 4.58 (1H, d, J=11.0 Hz, NH), 4.00 (1H, t, J=11 Hz, CHNH), 3.40-3.25 (2H, m), 2.98 (1H, m), 1.80-1.45 (22H, m), 0.80-0.70 (6H, m, CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06498196B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-882fa6f08b23434abe081172b1f13f21 |
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| Source note | uspto-grants-2002_12 |
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