HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080885Generated: November 1, 2026
Trimethyl orthoformate → HCID 67103487, compound
https://huagongshe.com/reaction/2080885
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | tert-Butyl hydrogen ((4-formylphenyl)methyl)carbonimidate | HCID 2794832 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 23155392 | HCID 23155392 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67103487 | HCID 67103487 | 90.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932281B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-7cb21eca34714b498ccd5ba959645c4b |
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| Source note | uspto-grants-2011_04 |
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