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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691968Generated: October 30, 2026

Tributylamine → HCID 178422984, compound

https://huagongshe.com/reaction/1691968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylamineHCID 7622—
ReactantSodium HydroxideHCID 14798—
ReactantThionyl ChlorideHCID 24386—
ReactantN,2-dihydroxy-4-methylbenzamideHCID 23021540—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 178422984HCID 17842298489.9%

Reaction Steps

50.0 g of N,2-dihydroxy-4-methylbenzamide was added to 350 mL of tert-butylmethylether, and 38.1 g of thionyl chloride was added dropwise at −1-0° C. This was stirred for 30 minutes at the same temperature. Then, 164 mL of tributylamine was added dropwise at −5-−3° C., and this was stirred for 1.5 hours at −5-5° C. To the reaction mixture, 200 mL of 20% sodium hydroxide aqueous solution was added, an organic layer was separated, and 100 mL of water, 42 mL of 20% sodium hydroxide aqueous solution and 5.0 g of celite were added. After insoluble matter was filtered off, the cake was washed with 100 mL of water. The filtrate and the washing solution were combined and an aqueous layer was separated. To the aqueous layer, 10 mL of acetone and 50 mL of acetic acid were added at 40-50° C. After stirring at the same temperature for 30 minutes, solids were filtered to obtain 40.1 g of 6-methyl-1,2-benzisoxazol-3-ol in the form of a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153816B2
Source datasetuspto-grants-2012_04
ORD IDord-ea60d4393317463ea8b3faf668f9496e
Source noteuspto-grants-2012_04