HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921669Generated: October 30, 2026
Lithium iodide → Tert-butyl 4-(1-aminocyclopropyl)benzoate
https://huagongshe.com/reaction/1921669
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium iodide | HCID 66321 | — |
| Reactant | Tert-butyl 4-cyanobenzoate | HCID 271408 | — |
| Reactant | Lithium propan-2-olate | HCID 23673350 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Catalyst | HCID 178459133 | HCID 178459133 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Tert-butyl 4-(1-aminocyclopropyl)benzoate | HCID 59305811 | — |
Reaction Steps
50 mL of a 2M lithium isopropoxide solution in THF was placed under an argon atmosphere and 13.4 g of anhydrous lithium iodide was added thereto. After 15 minutes, 45 mL of a 1M methyltitanium isopropoxide solution in THF was added. Then the mixture was combined with 8.1 g of tert-butyl 4-cyanobenzoate and stirred for 10 minutes. Then within 60 minutes, 47.3 mL of a 15% diethylzinc solution in hexane was added thereto and the mixture was stirred for 12 hours at RT. After hydrolysis with 20 mL of water, it was stirred for a further 30 minutes, filtered off, and washed 3× with 100 mL of ether. After extraction of the organic phase with water, the mixture was evaporated down with silica gel and the substance was chromatographed with dichloromethane/methanol (98:2) at 20 mL/min on silica gel 70. Residue: 3 g oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08173699B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-a90a8568033f448e96b5a8f58a54447f |
|---|
| Source note | uspto-grants-2012_05 |
|---|