HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597066Generated: October 27, 2026
Boron trifluoride etherate → HCID 21449337, compound
https://huagongshe.com/reaction/597066
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 1-(7-Chloroquinazolin-4-yl)-5-methoxy-2-methylindol-3-ylacetic acid | HCID 10194003 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21449337 | HCID 21449337 | — |
Reaction Steps
To a solution of 1-(7-chloroquinazolin-4-yl)-5-methoxy-2-methylindol-3-ylacetic acid (1.0g.) in dry methanol (50ml.) was added freshly distilled boron trifluoride etherate (0.5ml.), and the dark red solution was heated under reflux for 30 mins. To the solution was added saturated sodium acetate solution (5ml.), and the mixture was concentrated in vacuo. The residual mixture was shaken with a mixture of water (50ml.) and chloroform (30ml.). The aqueous layer was separated and extracted with further chloroform (2 × 20 ml.), and the combined extracts were washed successively with saturated sodium hydrogen carbonate solution (2 × 20ml.), water (10ml.) and saturated sodium chloride solution (15ml.). After drying, the extracts were evaporated to give methyl 1(7-chloroquinazolin-4-yl)-5-methoxy-2-methylindol-3-ylacetate, m.p. 111°-113° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04012513 |
|---|
| Source dataset | uspto-grants-1977_03 |
|---|
| ORD ID | ord-584902398f454e8d96826209bbb86b6d |
|---|
| Source note | uspto-grants-1977_03 |
|---|