HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl (triphenylphosphoranylidene) acetate → methyl E-4-[5-[2-(t-butoxycarbonyl)vinyl]-1-propylindol-3-ylmethyl]-3-methoxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl (triphenylphosphoranylidene) acetate | HCID 256127 | — |
| Reactant | Methyl 4-(5-formyl-1-propylindol-3-ylmethyl)-3-methoxybenzoate | HCID 14882683 | — |
| Product | methyl E-4-[5-[2-(t-butoxycarbonyl)vinyl]-1-propylindol-3-ylmethyl]-3-methoxybenzoate | HCID 19994980 | — |
Reaction Steps
Using a similar procedure to that described in Example 8, part e, except starting from methyl 4-(5-formyl-1-propylindol-3-ylmethyl)-3-methoxybenzoate, and using tert-butyl (triphenylphosphoranylidene)acetate, methyl E-4-[5-[2-(t-butoxycarbonyl)vinyl]-1-propylindol-3-ylmethyl]-3-methoxybenzoate was obtained (98%) as a viscous oil; partial NMR (250 MHz, DMSO-d6): 0.81(t, 3H, CH2CH3), 1.48(s, 9H, C(CH3)3), 1.75(m, 2H, CH2CH3), 3.82(s, 3H, OCH3), 3.91(s, 3H, OCH3), 6.38(d, J=15.8 Hz, 1H, CH=CH), 7.6(d, J=15.8 Hz, 1H, CH=CH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05041460 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-066baca738314b7e99c3d18c290fb0f9 |
| Source note | uspto-grants-1991_08 |