HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412617Generated: November 3, 2026
3-Chloro-1,2-propanediol → HCID 12800005, compound
https://huagongshe.com/reaction/2412617
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Chloro-1,2-propanediol | HCID 7290 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 12799968 | HCID 12799968 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12800005 | HCID 12800005 | 60.3% |
Reaction Steps
Sodium hydride (0.32 g of a 50% oil dispersion) was added to a stirred solution of (RS)-2-(n-decyl)indoline-6-carboxylic acid (2 g; prepared as described hereinbefore in Example 57) in dry dimethylformamide (50 ml). When the addition was complete, the mixture was warmed on the steam bath for 1 hour with stirring, and 3-chloro-1,2-propanediol (0.8 g) was added. The mixture was warmed on the steam bath for 20 hours with stirring. The solvent was then evaporated to dryness and the residue was dissolved in dichloromethane. The solution in dichloromethane was washed with water, dried over magnesium sulphate and filtered, and the solvent evaporated to dryness to give an oil which slowly solidified. This solid was washed with petroleum ether (b.p. 60°-80° C.), filtered off and dried in air to give (RS)(RS)-2,3-dihydroxyprop-1-yl 2-(n-decyl)indoline-6-carboxylate (1.5 g), in the form of an off-white powder m.p. 102°-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04493843 |
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| Source dataset | uspto-grants-1985_01 |
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| ORD ID | ord-2fecaa621492482dbfcc8727c8b52a33 |
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| Source note | uspto-grants-1985_01 |
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