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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080885Generated: November 1, 2026

Trimethyl orthoformate → HCID 67103487, compound

https://huagongshe.com/reaction/2080885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
Reactanttert-Butyl hydrogen ((4-formylphenyl)methyl)carbonimidateHCID 2794832—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23155392HCID 23155392—
SolventMethanolHCID 887—
ProductHCID 67103487HCID 6710348790.3%

Reaction Steps

The compound (81.0 mg) obtained in Example 90-3 was dissolved in anhydrous methanol (2.0 ml) and added with trimethyl orthoformate (94.1 μl) and the compound (101 mg) obtained in Example 23-3 and the whole was stirred overnight at room temperature under a nitrogen atmosphere. Subsequently, sodium borohydride (32.6 mg) was added thereto in an ice bath and the whole was stirred at room temperature for 1 hour. After completion of the reaction, the solvent was distilled off. The resultant was dissolved in chloroform and added with distilled water and the whole was stirred for a while. The resultant was subjected to extraction with chloroform and washed with a saturated saline solution. The organic layer was dried with anhydrous sodium sulfate. The solvent was distilled off, thereby obtaining the subject compound (158 mg) as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932281B2
Source datasetuspto-grants-2011_04
ORD IDord-7cb21eca34714b498ccd5ba959645c4b
Source noteuspto-grants-2011_04