Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 59238593 | HCID 59238593 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1046832-12-5 | HCID 59238644 | — |
Reaction Steps
To a cooled (0-5° C.) mixture of 11 (10.00 g, 41.44 mmol) and water (47 mL) was added 7 N aqueous HCl (47 ml, 331.50 mmol). Cooling bath was then removed and the reaction mixture was stirred at RT overnight. Then, the reaction mixture was basified to pH 9 by dropwise addition of 50% aqueous NaOH while maintaining the internal temperature <35° C. with an ice bath. The mixture was extracted with EtOAc (2×73 mL) followed by CH2Cl2 (2×71 mL). The organic extracts were dried (MgSO4) filtered and concentrated in vacuo to give a white residue that was recrystallised from CH2Cl2/hexane to afford (VII-n) (6.75 g, 83%) as a white crystalline solid; 1H NMR (400 MHz, CDCl3) δ 0.99 (s, 3H), 1.61 (td, J=13.9, 4.3 Hz, 2H), 2.09-2.19 (m, 4H), 2.55-2.65 (m, 6H), 3.74 (t, J=4.6 Hz, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178552B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-6dcc5c26cb78437b84e610dd8b8c84bc |
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| Source note | uspto-grants-2012_05 |
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