HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242340Generated: November 1, 2026
4-Chlorobenzenesulfonyl chloride → HCID 25263461, compound
https://huagongshe.com/reaction/2242340
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (2S)-2-Amino-3,3-dimethyl-1-butanol | HCID 2734079 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 25263461 | HCID 25263461 | — |
Reaction Steps
To a solution of S-tert-leucinol (0.20 g, 1.70 mmol), triethylamine (0.19 g, 1.87 mmol) and methylene chloride (10 mL) at 0° C., was added a solution of 4-chloro benzenesulfonyl chloride (0.36 g, 1.70 mmol) in CH2Cl2 (5 mL). After 15 minutes the ice bath was removed and the reaction allowed to reach 25° C. After 16 hours, the reaction was quenched by pouring into saturated sodium bicarbonate solution (20 mL) and additional methylene chloride (15 mL). The organic phase was separated and washed sequentially with 1N HCl solution (20 mL), distilled water and brine, dried over MgSO4 and evaporated to give the desired product as a white solid, mp 128-130° C. (0.46 g, 94%). MS (+APCI) 292.06 ([M+H]+). Anal. Calc'd for C12H18ClNO3S: C, 49.39; H, 6.22; N, 4.80. Found: C, 49.40; H, 6.17; N, 4.79.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07671075B2 |
|---|
| Source dataset | uspto-grants-2010_03 |
|---|
| ORD ID | ord-de92cd0e324c4bf6a2220512d23b4b36 |
|---|
| Source note | uspto-grants-2010_03 |
|---|