HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromomethyl acetate → HCID 78324451, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromomethyl acetate | HCID 68536 | — |
| Reactant | Iodomethyl pivalate | HCID 104401 | — |
| Reactant | HCID 78324148 | HCID 78324148 | — |
| Product | HCID 78324451 | HCID 78324451 | — |
Reaction Steps
This compound was synthesized by the same procedure used for the synthesis of (2S,3S,4R,5R,6S)-2-((bis((pivaloyloxy)methoxy)phosphoryl)methyl)-6-methyltetrahydro-2H-pyran-3,4,5-triyl triacetate, but using bromomethyl acetate (commercially available from Sigma Aldrich) instead of iodomethyl pivalate: ESI (M+H) 513.0; calc for C19H29O14P 512.4; 1H NMR (400 MHz, CD3OD) δ ppm 5.71-5.61 (m, 4 H) 5.29 (dd, J=3.33, 0.78 Hz, 1 H) 5.12 (dd, J=3.33, 10.17 Hz, 1 H) 5.05 (dd, J=9.59, 9.98 Hz, 1 H) 4.00-3.83 (m, 2 H) 2.35-2.17 (m, 2 H) 2.18 (s, 3 H) 2.16 (s, 3 H) 2.15 (s, 3 H) 2.09 (s, 3 H) 1.96 (2, 3 H) 1.18 (d, J=6.46 Hz, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09328134B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-652c00e6ac484751903f9d66a01fbe37 |
| Source note | uspto-grants-2016_05 |