HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409479Generated: October 27, 2026
Acetonitrile--water (1/1) → (+)-(1R,2S,5R)-5-(hydroxymethyl)cyclopent-3-ene-1,2-diyl dibenzoate
https://huagongshe.com/reaction/1409479
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | (1R,2S,3R,5R)-3-Amino-5-(hydroxymethyl)cyclopentane-1,2-diyl dibenzoate hydrochloride | HCID 66797769 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (+)-(1R,2S,5R)-5-(hydroxymethyl)cyclopent-3-ene-1,2-diyl dibenzoate | HCID 86693876 | — |
Reaction Steps
To a well stirred solution of (−)-(1R,2S,3R,5R)-3-amino-5-(hydroxymethyl)cyclopentane-1,2-diyl dibenzoate hydrochloride (6) (10.0 g, 25.5 mmol) in mixture of acetonitrile/water (1:1) was added sodium nitrite (8.8 g, 127.8 mmol) by portion wise at 0° C. After 15 minutes 50% aqueous acetic acid solution was added drop wise over a period of 0.5 hr and the mixture was vigorously stirred for 2 hr. The organic solvent was removed under reduced pressure and the rest of mixture was quenched with water. The aqueous phase was extracted with EtOAc (50 mL×3). The combined organic layers were dried over Na2SO4, filtered and the solvent was removed under reduced pressure. The residue was purified by flash silica gel column chromatography (20% EtOAc/hexane) to give compound 7. [α]24D −156° (c 1.0, CHCl3); 1H NMR (500 MHz, DMSO-d6): δ 8.05 (m, 2H), 7.89 (m, 2H), 7.52 (m, 2H), 7.38 (m, 2H), 7.28 (m, 2H), 6.11 (m, 3H), 5.54 (m, 1H), 3.87-3.82 (m, 2H), 3.27 (m, 1H), 2.29 (m, 1H). HR-MS Calcd. For (C25H29NO7+H)+ 339.1154. found 339.1286.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921384B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-a6610434b16a479287a5a8d896395071 |
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| Source note | uspto-grants-2014_12 |
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