HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900284Generated: October 26, 2026
Succinic anhydride → N-Butyl-N-(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)-succinamic Acid
https://huagongshe.com/reaction/1900284
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Butylamino-1-cyclohexyloxy-2,2,6,6-tetramethylpiperidine | HCID 21182129 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-Butyl-N-(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)-succinamic Acid | HCID 23372132 | 46% |
Reaction Steps
A solution of 10.2 grams (33 mmol) of 4-n-butylamino-1-cyclohexyloxy-2,2,6,6-tetramethylpiperidine (prepared in Example 8), 3.3 grams (33 mmol) of triethylamine, and 30 ml of tetrahydrofuran is added to a solution of 3.0 grams (30 mmol) of succinic anhydride in 20 ml of tetrahydrofuran over a 5-minute period. The reaction mixture is stirred for six hours and then diluted with ethyl acetate (200 ml). The organic solution is washed with 1N hydrochloric acid (2×50 ml), washed with water (50 ml), washed with saturated sodium chloride solution (50 ml), dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give an oil which crystallizes on standing. Recrystallization from heptane affords 5.6 grams (46% yield) of the title compound as a white solid melting at 110°-113° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05574162 |
|---|
| Source dataset | uspto-grants-1996_11 |
|---|
| ORD ID | ord-eb6ced63f7224a94bb0719d88c388788 |
|---|
| Source note | uspto-grants-1996_11 |
|---|