HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069458Generated: October 29, 2026
3-Methylbutanal → 4-[(4-Benzyloxy-phenyl)-(3-methyl-butyl)-amino]-piperidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1069458
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Methylbutanal | HCID 11552 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 4-(4-Benzyloxy-phenylamino)-piperidine-1-carboxylic acid tert-butyl ester | HCID 10547949 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[(4-Benzyloxy-phenyl)-(3-methyl-butyl)-amino]-piperidine-1-carboxylic acid tert-butyl ester | HCID 53712168 | 85.1% |
Reaction Steps
4-(4-Benzyloxy-phenylamino)-piperidine-1-carboxylic acid tert-butyl ester (9.51 g, 24.9 mmol) was dissolved in CH2Cl2 (150 mL) and treated with isovaleraldehyde (2.7 mL, 24.9 mmol). The reaction was stirred for 30 minutes, then cooled to 0° C., treated with NaBH(OAc)3, allowed to warm to room temperature as the ice melted, and stir overnight. The reaction was diluted with CH2Cl2 (300 mL), washed twice with saturated sodium bicarbonate solution and once with brine, dried over Na2SO4, and concentrated. The crude material was chromatographed on silica gel eluting with 4% MeOH/CH2Cl2 to give 9.59 g (85%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06251918B1 |
|---|
| Source dataset | uspto-grants-2001_06 |
|---|
| ORD ID | ord-c00c318390c94f2fac380d372c08d690 |
|---|
| Source note | uspto-grants-2001_06 |
|---|