Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 15285890 | HCID 15285890 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 9820836 | HCID 9820836 | 93.4% |
Reaction Steps
To a solution of 95 mg (0.23 mmol) of ethyl 4-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthylsulfonyl)benzoate (Compound 4) in 4.0 mL of tetrahydrofuran was added 1.0 mL of LiOH (2.6N aqueous solution) and 1.4 mL of MeOH. The solution was heated at 55° C. for 2.5 h, cooled to room temperature and concentrated in vacuo. The residue was diluted with brine, acidified to pH=1 using 10% HCl and extracted with ether (2×). The combined organic layers were washed with brine, dried (MgSO4), filtered and the solvents were removed in vacuo to give the title compound as a white solid (80 mg, 91%):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05672710 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-3a71a0eb6de144f0b00c4cd4d6ba7659 |
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| Source note | uspto-grants-1997_09 |
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