HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-tert-Butyl 2-(phenoxymethyl)pyrrolidine-1-carboxylate → (S)-tert-Butyl 2-(phenoxymethyl)azetidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-tert-Butyl 2-(phenoxymethyl)pyrrolidine-1-carboxylate | HCID 10636271 | — |
| Reactant | (S)-tert-Butyl 2-((tosyloxy)methyl)azetidine-1-carboxylate | HCID 11602568 | — |
| Product | (S)-tert-Butyl 2-(phenoxymethyl)azetidine-1-carboxylate | HCID 11565179 | 79% |
Reaction Steps
(S)-tert-Butyl 2-(phenoxymethyl)azetidine-1-carboxylate (16) was prepared according to the same procedure for compound 9, except using compound 15, and purified with hexanes-ether (2:1) to afford 0.81 g (79%) of 16 as a colorless oil. 1H NMR (300 MHz, CDCl3) δ CDCl3 7.30 (m, 2H), 6.94 (m, 3H), 4.53 (m, 1H), 4.26 (m, 1H), 4.12 (m, 1H), 3.93 (m, 2H), 2.33 (m, 2H), 1.43 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08329686B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-687d2629b79e49d895b356b5cee81d8f |
| Source note | uspto-grants-2012_12 |