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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491877Generated: October 27, 2026

(Phenylmethoxy)acetaldehyde → HCID 178525080, compound

https://huagongshe.com/reaction/491877

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Phenylmethoxy)acetaldehydeHCID 108989—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 178511568HCID 178511568—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 178525080HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531545B2
Source datasetuspto-grants-2009_05
ORD IDord-ec3421a9a983457884dfa3b5b404f698
Source noteuspto-grants-2009_05