HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061584Generated: November 1, 2026
4-Chlorobenzenesulfonyl chloride → HCID 59679493, compound
https://huagongshe.com/reaction/2061584
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 59679469 | HCID 59679469 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59679493 | HCID 59679493 | 88.4% |
Reaction Steps
7-Oxo-9-aza-bicyclo[3.3.1]nonane-3-carboxylic acid ethyl ester (4) (5.91 g, 27.9 mmol) was dissolved in CH2Cl2 (60 mL). Et3N (7.76 mL, 55.9 mmol) and 4-chlorobenzenesulfonyl chloride (5) (7.08 g, 33.6 mmol) were added and the reaction mixture was stirred at room temperature for 2 h. The reaction mixture was diluted with CH2Cl2 (50 mL) and washed with saturated NaHCO3 (50 mL). The aqueous phase was separated and extracted once with CH2Cl2 (50 mL). The combined organic phases were then dried (Na2SO4), filtered, concentrated under vacuum and the residue was purified on a silica gel column (eluant hexane/EtOAc, 9/1 to 1/1) to give 9.52 g (88%) of 9-(4-chloro-benzenesulfonyl)-7-oxo-9-aza-bicyclo[3.3.1]nonane-3-carboxylic acid ethyl ester (6). Retention time (min)=2.100, method [1], MS (ESI) 408.1 (M+Na); 1H NMR (CDCl3) δ 7.81 (d, J=8.2 Hz, 2H), 7.51 (d, J=8.2 Hz, 2H), 4.61-4.57 (m, 2H), 4.09 (q, J=7.1 Hz, 2H), 2.80 (dd, J=17.0, 7.1 Hz, 2H), 2.67-2.51 (m, 1H), 2.41 (d, J=16.4 Hz, 2H), 1.99-1.90 (m, 2H), 1.80 (dt, J=13.2, 4.4 Hz, 2H), 1.20 (t, J=7.1 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08283358B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-5a0c3f1767cf46d68f511da5bfcf311c |
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| Source note | uspto-grants-2012_10 |
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