HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731730Generated: November 1, 2026
Trimethyl orthoformate → HCID 13746853, compound
https://huagongshe.com/reaction/1731730
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | 1-Decyne | HCID 12997 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 13746853 | HCID 13746853 | — |
Reaction Steps
To freshly prepared ethyl magnesium bromide (from 61 mmoles bromoethane and 63 mmoles magnesium) was added 1-decyne (50 mmoles) in diethyl ether (10 ml) dropwise at ambient temperature. The reaction mixture was then heated at reflux for 2 hours. After cooling the reaction mixture, trimethylorthoformate (75 mmoles) in diethyl ether (10 ml) was added and the resultant mixture heated to distill off the diethyl ether. The resultant paste was taken up in anhydrous toluene (50 ml) and heated at reflux for 1 hour. The reaction mixture was poured into saturated ammonium chloride (50 ml) and then extracted with diethyl ether (3×50 ml). The organic phase was washed with water (3×20 ml) and dried over anhydrous magnesium sulfate. Evaporation of the organic phase afforded the desired product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04623535 |
|---|
| Source dataset | uspto-grants-1986_11 |
|---|
| ORD ID | ord-9aa4a599ffac4524bd714a62afd62fbd |
|---|
| Source note | uspto-grants-1986_11 |
|---|