HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Phenylmethoxy)acetaldehyde → HCID 178525080, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Phenylmethoxy)acetaldehyde | HCID 108989 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 178511568 | HCID 178511568 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 178525080 | HCID 178525080 | — |
Reaction Steps
A solution of cis-4-amino-cyclohexanecarboxylic acid benzyl ester (8 g, 34 mmol) and benzyloxyacetaldehyde (4.8 mL, 34 mmol) in 1,2-dichloroethane (2 L), was stirred at room temperature overnight. Then NaBH(OAc)3 (11 g, 51 mmol) was added and the reaction mixture was stirred at room temperature for 2 hours. Most of the solvent was then removed by vacuum. EtOAc (1 L) was added, and the resulting solution as washed with brine. The organic layer was dried over MgSO4, filtered, and evaporated to yield a residue. The residue was purified by column chromatography with flash silica gel (1:1 heptane/EtOAc) to yield cis-4-(2-benzyloxy-ethylamino)-cyclohexanecarboxylic acid benzyl ester as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531545B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-ec3421a9a983457884dfa3b5b404f698 |
| Source note | uspto-grants-2009_05 |