HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylbenzyl chloride → HCID 54503915, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylbenzyl chloride | HCID 7722 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | 2-[2-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]ethyl]-2H-1,4-benzoxazin-3(4H)-one | HCID 12048020 | — |
| Product | HCID 54503915 | HCID 54503915 | — |
Reaction Steps
Prepared from 2-(2-tert-butyldimethylsiloxyethyl)-3,4-dihydro-3-oxo-2H-1,4-benzoxazine by Methods F and G alkylating with 4-methylbenzyl chloride, in 50% overall yield. This material was crystallized from ether to afford a white solid, mp 92°-94° C.; IR (KBr) 3496, 1659, 1503, 1405, 1304, 1283, 1248, 1063, 801 cm-1 ; 1H NMR (CDCl3) δ2.18-2.36 (m, 5H), 3.91 (q, J=5.7, 2H), 4.83 (dd, J=7.4, 5.7, 1H), 5.12 (s, 2H), 6.90-7.00 (m, 4H), 7.13 (s, 4H); MH+ at m/z=298; Anal. Calc'd for C18H19NO3 : C, 72.71; H, 6.44; N, 4.71. Found: C, 72.71; H, 6.48; N, 4.65.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05696117 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-18303779ef114ab9ab9746e81b5e5566 |
| Source note | uspto-grants-1997_12 |