HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866478Generated: October 30, 2026
Benzene ethyl acetate → HCID 131711146, compound
https://huagongshe.com/reaction/866478
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene ethyl acetate | HCID 21583983 | — |
| Reactant | HCID 131711144 | HCID 131711144 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131711146 | HCID 131711146 | 30.8% |
Reaction Steps
A mixture of p-methoxybenzyl 7α-azido-3-methanesulfonyloxy-3-methyl-cepham-4-carboxylate (210 mg., 0.46 mMol), EM silica gel 60 (2.5 g.), and 3:1 PhH-EtOAc (5 ml.) is stirred in a capped flask at room temperature for 93 hrs. The mixture is diluted with EtOAc and filtered. The silica gel is washed with more EtOAc. The filtrate and washings are combined, washed with 5% NaHCO3 and brine, dried with MgSO4, filtered, and evaporated in vacuo to a pale yellow oil (158 mg.). The material is purified by plc on a 1000μ × 20 × 20 cm silica gel GF plate using 9:1 PhH-EtOAc as developing solvent. Two major uv visible bands are removed and eluted with EtOAc to yield the products. Band A (Rf 0.47) provides p-methoxybenzyl 7α-azido-3-methyl-ceph-3-em-4-carboxylate (51 mg.) as an oil. Band B (Rf 0.26) yields 6α-azido-2-methyl-2-hydroxymethyl-penam-3-carboxylic acid lactone (27 mg.) as an oil which crystallizes from CHCl3 : mp 164°-166° C. (micro hot stage); ir (Nujol) 4.76, 5.57, 5.67, 7.74, 8.32, and 9.79μ; nmr (100 MHz, DMSO-d6) δ1.59 (s, 3, CH3), 4.30 and 4.52 (ABq, 2, J=10Hz, CH2O), 5.20 (d, l, J=1.8Hz, H5 or H6), 5.28 (s, l, H3) and 5.29 (d, l, J=1.8Hz, H6 or H5); mass spectrum, m/e 240 (M+), 212, and 157.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04099000 |
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| Source dataset | uspto-grants-1978_07 |
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| ORD ID | ord-b654f213386542a09c9cfca08911626c |
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| Source note | uspto-grants-1978_07 |
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