HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088983Generated: November 4, 2026
2-((Tert-butoxy)carbonyl)-1,2,3,4-tetrahydroisoquinoline-7-carboxylic acid → HCID 58398107, compound
https://huagongshe.com/reaction/2088983
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-((Tert-butoxy)carbonyl)-1,2,3,4-tetrahydroisoquinoline-7-carboxylic acid | HCID 18988374 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58398107 | HCID 58398107 | — |
Reaction Steps
To a solution of 2-(tert-butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-7-carboxylic acid (0.689 g, 2.48 mmol) in THF (6 mL) at 0° C. was added LAH (4.97 mL of 1.0 M in THF, 4.97 mmol) dropwise under nitrogen. The reaction mixture was allowed to stir for 2 hours at 0° C., and then quenched with saturated aqueous ammonium chloride solution. The mixture was partitioned between water and EtOAc. The aqueous layer was extracted three times with EtOAc. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to provide tert-butyl 7-(hydroxymethyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08436016B2 |
|---|
| Source dataset | uspto-grants-2013_05 |
|---|
| ORD ID | ord-689142755b714d2394184a683d8e7cd0 |
|---|
| Source note | uspto-grants-2013_05 |
|---|