Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 70386519 | HCID 70386519 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 53707100 | HCID 53707100 | 91.3% |
Reaction Steps
A solution of the triester (28) (150 mg, 0.30 mmol) in dry ether (3 ml) was treated with lithium aluminium hydride (46 mg, 1.41 mmol) at room temperature. After 5 min ethyl acetate (1 ml) and then dilute hydrochloric acid (1 ml) was added, and the mixture was worked up with ether in the usual manner. Chromatography of the crude product on silica (2 g) eluted with ethyl acetate gave the product (6D) (79 mg, 91%), m.p. 229°-232° C. (from acetone), νmax (KBr disc) 3500 cm-1 (OH), δ (MeOH) (250 MHz) 7.41 (1 H, dd, J 2.5 and 1 Hz, 1-proton), 7.39 (1 H, d, J 8 Hz, 4-proton), 6.86 (1 H, ddd, J 8, 2.5, and 1 Hz, 3-proton), 4.11 (1 H, dt, J 10.5 and 5 Hz, 11-proton), 3.67 (1 H, t, J 8.5 Hz, 17-proton), 3.68 (2 H, t, J 9 Hz, 6-protons), 2.21 (1 H, A part of ABX system, JAX =5 Hz, JAX =12 Hz), 2.20-1.20 (13 H, m), 0.74 (3 H, s, 18-CH3),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04882439 |
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| Source dataset | uspto-grants-1989_11 |
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| ORD ID | ord-7f6b97ef53ff406d93dc3a96efd0fd08 |
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| Source note | uspto-grants-1989_11 |
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