HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424603Generated: November 4, 2026
Lithium hydroxide, monohydrate → HCID 46216689, compound
https://huagongshe.com/reaction/1424603
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | HCID 25064817 | HCID 25064817 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 46216689 | HCID 46216689 | — |
Reaction Steps
To a solution of ethyl 2-(7-bromo-1′-((2-adamantyl)carbamoyl)-2,3-dihydrospiro[indene-1,4′-piperidine]-3-yl)acetate, isomer 2 (1.57 g, 3 mmol) in ethanol (15 mL) was added 2 M aq LiOH.H2O (15 mL, 30 mmol) at 0° C. and the mixture was stirred overnight at rt. The reaction mixture was washed with 1 aq N HCl until pH=5-6. The combined organic layers were dried over Na2SO4, filtered and concentrated to obtain 2-(7-bromo-1′-((2-adamantyl)carbamoyl)-2,3-dihydrospiro[indene-1,4′-piperidine]-3-yl)acetic acid isomer 2 (1.33 g, 90%). LC-MS Method 5 tR=1.44 min, m/z=503.1; 1H NMR (CD3OD): δ=1.19-1.48 (m, 2H), 1.48-1.62 (m, 4H), 1.65-1.95 (m, 12H), 2.20-2.66 (m, 3H), 2.70-3.12 (m, 4H), 3.50 (m, 1H), 3.70-4.08 (m, 3H), 4.89 (m, 1H), 6.90-7.15 (m, 2H), 7.40 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08927715B2 |
|---|
| Source dataset | uspto-grants-2015_01 |
|---|
| ORD ID | ord-191c97a98762489aa3648b5e092522e4 |
|---|
| Source note | uspto-grants-2015_01 |
|---|